Trial Outcomes & Findings for A Safety and Efficacy Study of the Combination Estradiol and Progesterone to Treat Vasomotor Symptoms (NCT NCT01942668)
NCT ID: NCT01942668
Last Updated: 2019-05-06
Results Overview
Mean change in frequency of moderate to severe vasomotor symptoms from Baseline to Week 4. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of moderate to severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of moderate to severe hot flushes for the subject week.
COMPLETED
PHASE3
1845 participants
Baseline and Week 4
2019-05-06
Participant Flow
Participant milestones
| Measure |
Combined Estradiol 1 mg / Progesterone 100 mg
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 50 mg
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
Two Placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Overall Study
STARTED
|
418
|
426
|
422
|
427
|
152
|
|
Overall Study
COMPLETED
|
284
|
305
|
312
|
281
|
93
|
|
Overall Study
NOT COMPLETED
|
134
|
121
|
110
|
146
|
59
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
A Safety and Efficacy Study of the Combination Estradiol and Progesterone to Treat Vasomotor Symptoms
Baseline characteristics by cohort
| Measure |
Combined Estradiol 1 mg / Progesterone 100 mg
n=415 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=424 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=421 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=424 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=151 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Total
n=1835 Participants
Total of all reporting groups
|
|---|---|---|---|---|---|---|
|
Age, Categorical
<=18 years
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
0 Participants
n=7 Participants
|
0 Participants
n=31 Participants
|
0 Participants
n=30 Participants
|
|
Age, Categorical
Between 18 and 65 years
|
415 Participants
n=99 Participants
|
424 Participants
n=107 Participants
|
421 Participants
n=206 Participants
|
424 Participants
n=7 Participants
|
151 Participants
n=31 Participants
|
1835 Participants
n=30 Participants
|
|
Age, Categorical
>=65 years
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
0 Participants
n=7 Participants
|
0 Participants
n=31 Participants
|
0 Participants
n=30 Participants
|
|
Age, Continuous
|
54.7 years
STANDARD_DEVIATION 4.37 • n=99 Participants
|
54.5 years
STANDARD_DEVIATION 4.52 • n=107 Participants
|
54.9 years
STANDARD_DEVIATION 4.27 • n=206 Participants
|
54.4 years
STANDARD_DEVIATION 4.04 • n=7 Participants
|
54.5 years
STANDARD_DEVIATION 4.32 • n=31 Participants
|
54.6 years
STANDARD_DEVIATION 4.31 • n=30 Participants
|
|
Sex: Female, Male
Female
|
415 Participants
n=99 Participants
|
424 Participants
n=107 Participants
|
421 Participants
n=206 Participants
|
424 Participants
n=7 Participants
|
151 Participants
n=31 Participants
|
1835 Participants
n=30 Participants
|
|
Sex: Female, Male
Male
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
0 Participants
n=7 Participants
|
0 Participants
n=31 Participants
|
0 Participants
n=30 Participants
|
|
Region of Enrollment
United States
|
415 participants
n=99 Participants
|
424 participants
n=107 Participants
|
421 participants
n=206 Participants
|
424 participants
n=7 Participants
|
151 participants
n=31 Participants
|
1835 participants
n=30 Participants
|
PRIMARY outcome
Timeframe: Baseline and Week 4Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of moderate to severe vasomotor symptoms from Baseline to Week 4. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of moderate to severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of moderate to severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=142 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=152 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=126 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=134 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=144 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Co-Primary Efficacy Endpoint: Frequency of Moderate to Severe Vasomotor Symptoms (MITT-VMS)
|
-33.6 weekly hot flushes
Standard Deviation 30.64
|
-38.9 weekly hot flushes
Standard Deviation 31.04
|
-26.4 weekly hot flushes
Standard Deviation 27.05
|
-40.6 weekly hot flushes
Standard Deviation 30.59
|
-35.1 weekly hot flushes
Standard Deviation 29.14
|
PRIMARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of moderate to severe vasomotor symptoms from Baseline to Week 12. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of moderate to severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of moderate to severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=124 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=135 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=115 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=129 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Co-Primary Efficacy Endpoint: Frequency of Moderate to Severe Vasomotor Symptoms (MITT-VMS)
|
-50.2 weekly hot flushes
Standard Deviation 31.35
|
-52.4 weekly hot flushes
Standard Deviation 33.90
|
-40.2 weekly hot flushes
Standard Deviation 29.79
|
-55.1 weekly hot flushes
Standard Deviation 31.36
|
-53.7 weekly hot flushes
Standard Deviation 31.93
|
PRIMARY outcome
Timeframe: Baseline and Week 4Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of moderate to severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 4. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score = (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of moderate to severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=142 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=152 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=126 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=134 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=144 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Co-Primary Efficacy Endpoint: Severity of Moderate to Severe Vasomotor Symptoms (MITT-VMS)
|
-0.40 scores on a scale
Standard Deviation 0.469
|
-0.44 scores on a scale
Standard Deviation 0.514
|
-0.34 scores on a scale
Standard Deviation 0.386
|
-0.48 scores on a scale
Standard Deviation 0.547
|
-0.51 scores on a scale
Standard Deviation 0.563
|
PRIMARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of moderate to severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 12. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score = (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of moderate to severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=124 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=135 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=115 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=129 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Co-Primary Efficacy Endpoint: Severity of Moderate to Severe Vasomotor Symptoms (MITT-VMS)
|
-0.76 scores on a scale
Standard Deviation 0.744
|
-0.71 scores on a scale
Standard Deviation 0.806
|
-0.56 scores on a scale
Standard Deviation 0.603
|
-1.12 scores on a scale
Standard Deviation 0.963
|
-0.90 scores on a scale
Standard Deviation 0.783
|
PRIMARY outcome
Timeframe: Baseline and Month 12Population: Randomized subjects who had taken at least 1 capsule, had no major protocol violations, acceptable biopsy at baseline (evaluable tissue, no endometrial hyperplasia, polyp or cancer), had a biopsy at month 12 (on or after Study Day 326) or had a diagnosis of endometrial hyperplasia prior to month 12.
Endometrial biopsies centrally evaluated by 2 primary pathologists using criteria from Blaustein's Pathology text. Pathologists classified bx into 1 of following 3 categories: Cat.1: Non-endometrial malignancy/non-hyperplasia; Cat.2: Endometrial hyperplasia; Cat.3: Endometrial malignancy. Consensus reached when 2 primary pathologist agreed on any of above categories; if primary pathologists disagreed on presence of hyperplasia, result of 3rd pathologist was utilized and final decision regarding presence of hyperplasia was based on diagnosis of majority. If all 3 reads disparate, final diagnosis based on most severe dx. Incidence rate calculated as: I=A/B where I=incidence rate at M12 evaluation, A=all new subjects with biopsies positive for endometrial hyperplasia during study but post-Baseline, B=all subjects w/biopsies following M11 meeting criteria specified plus all subjects w/biopsies positive for endometrial hyperplasia by any pathologists before M11.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=306 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=274 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=92 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=280 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=303 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Primary Safety Endpoint: Endometrial Protection - Hyperplasia
|
0 Participants
|
0 Participants
|
0 Participants
|
0 Participants
|
0 Participants
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: Randomized subjects who had taken at least 1 capsule, had no major protocol violations, acceptable biopsy at baseline (evaluable tissue, no endometrial hyperplasia, polyp or cancer), had a biopsy at month 12 (on or after Study Day 326) or had a diagnosis of endometrial hyperplasia prior to month 12.
Endometrial biopsies centrally evaluated by 3 primary pathologists using criteria described in Blaustein's Pathology text. Pathologists classified biopsy into 1 of following 3 categories: Cat.1: Non-endometrial malignancy/non-hyperplasia; Cat.2: Endometrial hyperplasia; Cat.3: Endometrial malignancy. Consensus was reached when the 2 of 3 pathologist readers agreed on any of the above categories; if all three reads were disparate, the final diagnosis was based on the most severe diagnosis. Incidence rate calculated as: I=A/B where I=incidence rate at M12 evaluation, A=all new subjects with biopsies positive for endometrial hyperplasia during study but post-Baseline, B=all subjects with biopsies following M11 meeting the criteria specified plus all subjects with biopsies positive for endometrial hyperplasia by any of the pathologists before M11.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=306 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=274 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=92 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=280 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=303 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Endometrial Protection - Hyperplasia
|
0 Participants
|
0 Participants
|
0 Participants
|
0 Participants
|
0 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 1Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of moderate to severe vasomotor symptoms from Baseline to Week 1. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of moderate to severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of moderate to severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=145 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=154 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=134 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=138 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=149 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Moderate to Severe Vasomotor Symptoms - Week 1 (MITT-VMS)
|
-11.0 weekly hot flushes
Standard Deviation 20.94
|
-16.3 weekly hot flushes
Standard Deviation 22.28
|
-13.0 weekly hot flushes
Standard Deviation 21.25
|
-12.2 weekly hot flushes
Standard Deviation 20.10
|
-11.5 weekly hot flushes
Standard Deviation 20.19
|
SECONDARY outcome
Timeframe: Baseline and Week 2Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of moderate to severe vasomotor symptoms from Baseline to Week 2. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of moderate to severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of moderate to severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=145 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=153 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=133 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=134 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=146 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Moderate to Severe Vasomotor Symptoms - Week 2 (MITT-VMS)
|
-19.0 weekly hot flushes
Standard Deviation 28.32
|
-25.4 weekly hot flushes
Standard Deviation 26.63
|
-21.3 weekly hot flushes
Standard Deviation 24.75
|
-26.6 weekly hot flushes
Standard Deviation 27.67
|
-21.2 weekly hot flushes
Standard Deviation 24.79
|
SECONDARY outcome
Timeframe: Baseline and Week 3Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of moderate to severe vasomotor symptoms from Baseline to Week 3. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of moderate to severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of moderate to severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=144 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=153 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=131 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=136 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=144 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Moderate to Severe Vasomotor Symptoms - Week 3 (MITT-VMS)
|
-28.1 weekly hot flushes
Standard Deviation 28.18
|
-33.6 weekly hot flushes
Standard Deviation 27.76
|
-25.1 weekly hot flushes
Standard Deviation 27.26
|
-34.3 weekly hot flushes
Standard Deviation 29.22
|
-29.0 weekly hot flushes
Standard Deviation 26.73
|
SECONDARY outcome
Timeframe: Baseline and Week 4Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of moderate to severe vasomotor symptoms from Baseline to Week 4. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of moderate to severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of moderate to severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=142 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=152 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=126 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=134 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=144 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Moderate to Severe Vasomotor Symptoms - Week 4 (MITT-VMS)
|
-33.6 weekly hot flushes
Standard Deviation 30.64
|
-38.9 weekly hot flushes
Standard Deviation 31.04
|
-26.4 weekly hot flushes
Standard Deviation 27.05
|
-40.6 weekly hot flushes
Standard Deviation 30.59
|
-35.1 weekly hot flushes
Standard Deviation 29.14
|
SECONDARY outcome
Timeframe: Baseline and Week 5Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of moderate to severe vasomotor symptoms from Baseline to Week 5. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of moderate to severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of moderate to severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=139 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=147 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=124 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=131 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=143 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Moderate to Severe Vasomotor Symptoms - Week 5 (MITT-VMS)
|
-37.1 weekly hot flushes
Standard Deviation 30.64
|
-43.5 weekly hot flushes
Standard Deviation 33.31
|
-31.6 weekly hot flushes
Standard Deviation 28.96
|
-45.9 weekly hot flushes
Standard Deviation 32.31
|
-39.5 weekly hot flushes
Standard Deviation 28.53
|
SECONDARY outcome
Timeframe: Baseline and Week 6Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of moderate to severe vasomotor symptoms from Baseline to Week 6. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of moderate to severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of moderate to severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=139 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=146 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=123 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=132 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=143 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Moderate to Severe Vasomotor Symptoms - Week 6 (MITT-VMS)
|
-40.1 weekly hot flushes
Standard Deviation 33.62
|
-45.5 weekly hot flushes
Standard Deviation 33.14
|
-32.7 weekly hot flushes
Standard Deviation 28.53
|
-49.4 weekly hot flushes
Standard Deviation 32.76
|
-41.7 weekly hot flushes
Standard Deviation 29.97
|
SECONDARY outcome
Timeframe: Baseline and Week 7Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of moderate to severe vasomotor symptoms from Baseline to Week 7. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of moderate to severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of moderate to severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=139 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=147 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=120 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=130 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=142 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Moderate to Severe Vasomotor Symptoms - Week 7 (MITT-VMS)
|
-43.8 weekly hot flushes
Standard Deviation 33.20
|
-47.7 weekly hot flushes
Standard Deviation 32.18
|
-33.4 weekly hot flushes
Standard Deviation 29.37
|
-51.5 weekly hot flushes
Standard Deviation 31.51
|
-45.0 weekly hot flushes
Standard Deviation 30.73
|
SECONDARY outcome
Timeframe: Baseline and Week 8Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of moderate to severe vasomotor symptoms from Baseline to Week 8. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of moderate to severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of moderate to severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=137 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=147 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=120 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=129 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=140 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Moderate to Severe Vasomotor Symptoms - Week 8 (MITT-VMS)
|
-45.4 weekly hot flushes
Standard Deviation 32.55
|
-48.4 weekly hot flushes
Standard Deviation 32.82
|
-36.0 weekly hot flushes
Standard Deviation 30.66
|
-52.3 weekly hot flushes
Standard Deviation 31.63
|
-46.8 weekly hot flushes
Standard Deviation 30.64
|
SECONDARY outcome
Timeframe: Baseline and Week 9Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of moderate to severe vasomotor symptoms from Baseline to Week 9. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of moderate to severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of moderate to severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=132 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=141 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=119 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=137 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Moderate to Severe Vasomotor Symptoms - Week 9 (MITT-VMS)
|
-47.4 weekly hot flushes
Standard Deviation 30.13
|
-50.1 weekly hot flushes
Standard Deviation 33.92
|
-36.4 weekly hot flushes
Standard Deviation 29.09
|
-52.6 weekly hot flushes
Standard Deviation 32.57
|
-50.5 weekly hot flushes
Standard Deviation 31.01
|
SECONDARY outcome
Timeframe: Baseline and Week 10Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of moderate to severe vasomotor symptoms from Baseline to Week 10. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of moderate to severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of moderate to severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=129 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=140 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=118 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=126 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=133 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Moderate to Severe Vasomotor Symptoms - Week 10 (MITT-VMS)
|
-49.0 weekly hot flushes
Standard Deviation 30.24
|
-50.6 weekly hot flushes
Standard Deviation 33.36
|
-37.1 weekly hot flushes
Standard Deviation 29.74
|
-53.2 weekly hot flushes
Standard Deviation 32.58
|
-51.9 weekly hot flushes
Standard Deviation 32.79
|
SECONDARY outcome
Timeframe: Baseline and Week 11Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of moderate to severe vasomotor symptoms from Baseline to Week 11. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of moderate to severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of moderate to severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=129 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=137 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=118 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=126 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=134 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Moderate to Severe Vasomotor Symptoms - Week 11 (MITT-VMS)
|
-49.4 weekly hot flushes
Standard Deviation 30.71
|
-50.9 weekly hot flushes
Standard Deviation 34.33
|
-36.7 weekly hot flushes
Standard Deviation 30.32
|
-53.7 weekly hot flushes
Standard Deviation 32.21
|
-52.0 weekly hot flushes
Standard Deviation 31.24
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of moderate to severe vasomotor symptoms from Baseline to Week 12. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of moderate to severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of moderate to severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=124 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=135 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=115 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=129 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Moderate to Severe Vasomotor Symptoms - Week 12 (MITT-VMS)
|
-50.2 weekly hot flushes
Standard Deviation 31.35
|
-52.4 weekly hot flushes
Standard Deviation 33.90
|
-40.2 weekly hot flushes
Standard Deviation 29.79
|
-55.1 weekly hot flushes
Standard Deviation 31.36
|
-53.7 weekly hot flushes
Standard Deviation 31.93
|
SECONDARY outcome
Timeframe: Baseline and Week 1Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of moderate to severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 1. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score = (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of moderate to severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=145 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=154 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=134 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=138 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=149 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Moderate to Severe Vasomotor Symptoms - Week 1 (MITT-VMS)
|
-0.23 scores on a scale
Standard Deviation 0.264
|
-0.25 scores on a scale
Standard Deviation 0.327
|
-0.25 scores on a scale
Standard Deviation 0.257
|
-0.24 scores on a scale
Standard Deviation 0.305
|
-0.25 scores on a scale
Standard Deviation 0.270
|
SECONDARY outcome
Timeframe: Baseline and Week 2Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of moderate to severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 2. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score = (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of moderate to severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=145 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=153 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=133 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=134 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=146 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Moderate to Severe Vasomotor Symptoms - Week 2 (MITT-VMS)
|
-0.27 scores on a scale
Standard Deviation 0.354
|
-0.29 scores on a scale
Standard Deviation 0.314
|
-0.28 scores on a scale
Standard Deviation 0.310
|
-0.34 scores on a scale
Standard Deviation 0.411
|
-0.34 scores on a scale
Standard Deviation 0.390
|
SECONDARY outcome
Timeframe: Baseline and Week 3Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of moderate to severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 3. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score = (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of moderate to severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=144 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=153 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=131 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=136 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=144 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Moderate to Severe Vasomotor Symptoms - Week 3 (MITT-VMS)
|
-0.32 scores on a scale
Standard Deviation 0.410
|
-0.37 scores on a scale
Standard Deviation 0.424
|
-0.32 scores on a scale
Standard Deviation 0.372
|
-0.43 scores on a scale
Standard Deviation 0.514
|
-0.44 scores on a scale
Standard Deviation 0.437
|
SECONDARY outcome
Timeframe: Baseline and Week 4Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of moderate to severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 4. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score = (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of moderate to severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=142 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=152 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=126 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=134 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=144 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Moderate to Severe Vasomotor Symptoms - Week 4 (MITT-VMS)
|
-0.40 scores on a scale
Standard Deviation 0.469
|
-0.44 scores on a scale
Standard Deviation 0.514
|
-0.34 scores on a scale
Standard Deviation 0.386
|
-0.48 scores on a scale
Standard Deviation 0.547
|
-0.51 scores on a scale
Standard Deviation 0.563
|
SECONDARY outcome
Timeframe: Baseline and Week 5Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of moderate to severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 5. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score = (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of moderate to severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=139 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=147 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=124 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=131 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=143 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Moderate to Severe Vasomotor Symptoms - Week 5 (MITT-VMS)
|
-0.44 scores on a scale
Standard Deviation 0.463
|
-0.53 scores on a scale
Standard Deviation 0.610
|
-0.42 scores on a scale
Standard Deviation 0.551
|
-0.64 scores on a scale
Standard Deviation 0.702
|
-0.56 scores on a scale
Standard Deviation 0.558
|
SECONDARY outcome
Timeframe: Baseline and Week 6Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of moderate to severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 6. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score = (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of moderate to severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=139 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=146 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=123 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=132 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=143 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Moderate to Severe Vasomotor Symptoms - Week 6 (MITT-VMS)
|
-0.54 scores on a scale
Standard Deviation 0.578
|
-0.63 scores on a scale
Standard Deviation 0.763
|
-0.45 scores on a scale
Standard Deviation 0.573
|
-0.80 scores on a scale
Standard Deviation 0.840
|
-0.61 scores on a scale
Standard Deviation 0.640
|
SECONDARY outcome
Timeframe: Baseline and Week 7Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of moderate to severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 7. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score = (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of moderate to severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=139 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=147 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=120 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=130 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=142 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Moderate to Severe Vasomotor Symptoms - Week 7 (MITT-VMS)
|
-0.63 scores on a scale
Standard Deviation 0.637
|
-0.64 scores on a scale
Standard Deviation 0.764
|
-0.44 scores on a scale
Standard Deviation 0.483
|
-0.81 scores on a scale
Standard Deviation 0.793
|
-0.69 scores on a scale
Standard Deviation 0.694
|
SECONDARY outcome
Timeframe: Baseline and Week 8Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of moderate to severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 8. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score = (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of moderate to severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=137 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=147 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=120 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=129 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=140 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Moderate to Severe Vasomotor Symptoms - Week 8 (MITT-VMS)
|
-0.65 scores on a scale
Standard Deviation 0.685
|
-0.64 scores on a scale
Standard Deviation 0.745
|
-0.51 scores on a scale
Standard Deviation 0.563
|
-0.88 scores on a scale
Standard Deviation 0.854
|
-0.70 scores on a scale
Standard Deviation 0.642
|
SECONDARY outcome
Timeframe: Baseline and Week 9Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of moderate to severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 9. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score = (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of moderate to severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=132 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=141 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=119 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=137 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Moderate to Severe Vasomotor Symptoms - Week 9 (MITT-VMS)
|
-0.73 scores on a scale
Standard Deviation 0.720
|
-0.71 scores on a scale
Standard Deviation 0.772
|
-0.48 scores on a scale
Standard Deviation 0.536
|
-0.96 scores on a scale
Standard Deviation 0.892
|
-0.74 scores on a scale
Standard Deviation 0.699
|
SECONDARY outcome
Timeframe: Baseline and Week 10Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of moderate to severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 10. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score = (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of moderate to severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=129 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=140 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=118 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=126 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=133 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Moderate to Severe Vasomotor Symptoms - Week 10 (MITT-VMS)
|
-0.78 scores on a scale
Standard Deviation 0.769
|
-0.62 scores on a scale
Standard Deviation 0.739
|
-0.53 scores on a scale
Standard Deviation 0.575
|
-1.05 scores on a scale
Standard Deviation 0.953
|
-0.77 scores on a scale
Standard Deviation 0.727
|
SECONDARY outcome
Timeframe: Baseline and Week 11Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of moderate to severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 11. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score = (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of moderate to severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=129 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=137 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=118 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=126 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=134 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Moderate to Severe Vasomotor Symptoms - Week 11 (MITT-VMS)
|
-0.78 scores on a scale
Standard Deviation 0.782
|
-0.68 scores on a scale
Standard Deviation 0.767
|
-0.54 scores on a scale
Standard Deviation 0.566
|
-1.04 scores on a scale
Standard Deviation 0.931
|
-0.86 scores on a scale
Standard Deviation 0.777
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of moderate to severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 12. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score = (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of moderate to severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=124 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=135 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=115 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=129 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Moderate to Severe Vasomotor Symptoms - Week 12 (MITT-VMS)
|
-0.76 scores on a scale
Standard Deviation 0.744
|
-0.71 scores on a scale
Standard Deviation 0.806
|
-0.56 scores on a scale
Standard Deviation 0.603
|
-1.12 scores on a scale
Standard Deviation 0.963
|
-0.90 scores on a scale
Standard Deviation 0.783
|
SECONDARY outcome
Timeframe: Baseline and Week 1Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 1. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of mild, moderate and severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of mild, moderate and severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=145 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=154 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=134 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=138 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=149 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 1 (MITT-VMS)
|
-12.5 weekly hot flushes
Standard Deviation 24.62
|
-17.7 weekly hot flushes
Standard Deviation 27.78
|
-12.2 weekly hot flushes
Standard Deviation 23.76
|
-12.9 weekly hot flushes
Standard Deviation 22.12
|
-12.4 weekly hot flushes
Standard Deviation 23.94
|
SECONDARY outcome
Timeframe: Baseline and Week 2Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 2. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of mild, moderate and severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of mild, moderate and severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=145 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=153 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=133 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=134 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=146 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 2 (MITT-VMS)
|
-21.8 weekly hot flushes
Standard Deviation 31.66
|
-27.8 weekly hot flushes
Standard Deviation 32.35
|
-21.7 weekly hot flushes
Standard Deviation 27.45
|
-28.2 weekly hot flushes
Standard Deviation 29.45
|
-22.4 weekly hot flushes
Standard Deviation 30.53
|
SECONDARY outcome
Timeframe: Baseline and Week 3Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 3. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of mild, moderate and severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of mild, moderate and severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=144 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=153 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=131 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=136 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=144 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 3 (MITT-VMS)
|
-31.3 weekly hot flushes
Standard Deviation 30.79
|
-35.6 weekly hot flushes
Standard Deviation 33.52
|
-25.8 weekly hot flushes
Standard Deviation 30.41
|
-37.4 weekly hot flushes
Standard Deviation 32.33
|
-30.7 weekly hot flushes
Standard Deviation 32.00
|
SECONDARY outcome
Timeframe: Baseline and Week 4Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 4. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of mild, moderate and severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of mild, moderate and severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=142 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=152 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=126 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=134 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=144 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 4 (MITT-VMS)
|
-35.4 weekly hot flushes
Standard Deviation 34.58
|
-41.5 weekly hot flushes
Standard Deviation 37.40
|
-26.8 weekly hot flushes
Standard Deviation 30.52
|
-44.4 weekly hot flushes
Standard Deviation 34.53
|
-37.7 weekly hot flushes
Standard Deviation 35.38
|
SECONDARY outcome
Timeframe: Baseline and Week 5Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 5. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of mild, moderate and severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of mild, moderate and severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=139 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=147 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=124 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=131 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=143 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 5 (MITT-VMS)
|
-40.1 weekly hot flushes
Standard Deviation 32.52
|
-46.8 weekly hot flushes
Standard Deviation 39.88
|
-33.3 weekly hot flushes
Standard Deviation 33.49
|
-49.9 weekly hot flushes
Standard Deviation 33.86
|
-42.3 weekly hot flushes
Standard Deviation 34.15
|
SECONDARY outcome
Timeframe: Baseline and Week 6Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 6. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of mild, moderate and severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of mild, moderate and severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=139 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=146 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=123 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=132 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=143 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 6 (MITT-VMS)
|
-43.0 weekly hot flushes
Standard Deviation 34.84
|
-49.4 weekly hot flushes
Standard Deviation 40.28
|
-34.1 weekly hot flushes
Standard Deviation 33.32
|
-53.9 weekly hot flushes
Standard Deviation 35.34
|
-44.9 weekly hot flushes
Standard Deviation 36.12
|
SECONDARY outcome
Timeframe: Baseline and Week 7Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 7. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of mild, moderate and severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of mild, moderate and severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=139 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=147 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=120 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=130 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=142 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 7 (MITT-VMS)
|
-47.2 weekly hot flushes
Standard Deviation 34.39
|
-51.5 weekly hot flushes
Standard Deviation 39.69
|
-33.4 weekly hot flushes
Standard Deviation 33.71
|
-56.1 weekly hot flushes
Standard Deviation 34.55
|
-48.8 weekly hot flushes
Standard Deviation 36.92
|
SECONDARY outcome
Timeframe: Baseline and Week 8Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 8. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of mild, moderate and severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of mild, moderate and severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=137 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=147 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=120 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=129 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=140 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 8 (MITT-VMS)
|
-49.5 weekly hot flushes
Standard Deviation 34.34
|
-52.4 weekly hot flushes
Standard Deviation 40.65
|
-36.9 weekly hot flushes
Standard Deviation 35.53
|
-57.1 weekly hot flushes
Standard Deviation 35.91
|
-50.6 weekly hot flushes
Standard Deviation 37.73
|
SECONDARY outcome
Timeframe: Baseline and Week 9Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 9. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of mild, moderate and severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of mild, moderate and severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=132 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=141 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=119 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=137 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 9 (MITT-VMS)
|
-52.8 weekly hot flushes
Standard Deviation 33.68
|
-54.5 weekly hot flushes
Standard Deviation 41.89
|
-38.3 weekly hot flushes
Standard Deviation 35.04
|
-57.6 weekly hot flushes
Standard Deviation 36.43
|
-54.7 weekly hot flushes
Standard Deviation 38.76
|
SECONDARY outcome
Timeframe: Baseline and Week 10Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 10. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of mild, moderate and severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of mild, moderate and severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=129 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=140 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=118 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=126 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=133 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 10 (MITT-VMS)
|
-53.7 weekly hot flushes
Standard Deviation 34.39
|
-55.7 weekly hot flushes
Standard Deviation 41.55
|
-38.3 weekly hot flushes
Standard Deviation 35.52
|
-58.5 weekly hot flushes
Standard Deviation 36.86
|
-56.1 weekly hot flushes
Standard Deviation 39.97
|
SECONDARY outcome
Timeframe: Baseline and Week 11Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 11. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of mild, moderate and severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of mild, moderate and severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=129 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=137 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=118 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=126 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=134 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 11 (MITT-VMS)
|
-54.2 weekly hot flushes
Standard Deviation 34.38
|
-56.1 weekly hot flushes
Standard Deviation 42.45
|
-38.4 weekly hot flushes
Standard Deviation 35.85
|
-58.8 weekly hot flushes
Standard Deviation 36.58
|
-57.0 weekly hot flushes
Standard Deviation 38.81
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 12. The baseline was the most recent 7 consecutive days of data prior to randomization. The weekly frequency of mild, moderate and severe hot flushes was calculated from the daily diary record using a forward counting process of 7 day intervals beginning with the baseline date. Weekly frequency equals total number of mild, moderate and severe hot flushes for the subject week.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=124 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=135 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=115 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=129 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 12 (MITT-VMS)
|
-54.8 weekly hot flushes
Standard Deviation 34.94
|
-57.0 weekly hot flushes
Standard Deviation 41.71
|
-41.7 weekly hot flushes
Standard Deviation 36.35
|
-60.3 weekly hot flushes
Standard Deviation 36.42
|
-58.8 weekly hot flushes
Standard Deviation 39.59
|
SECONDARY outcome
Timeframe: Baseline and Week 1Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of mild, moderate and severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 1. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score =(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=145 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=154 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=134 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=138 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=149 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Mild, Moderate and Severe Vasomotor Symptoms - Week 1 (MITT-VMS)
|
-0.02 scores on a scale
Standard Deviation 0.197
|
-0.08 scores on a scale
Standard Deviation 0.305
|
-0.07 scores on a scale
Standard Deviation 0.200
|
-0.06 scores on a scale
Standard Deviation 0.211
|
-0.05 scores on a scale
Standard Deviation 0.206
|
SECONDARY outcome
Timeframe: Baseline and Week 2Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of mild, moderate and severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 2. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score =(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=145 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=153 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=133 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=134 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=146 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Mild, Moderate and Severe Vasomotor Symptoms - Week 2 (MITT-VMS)
|
-0.06 scores on a scale
Standard Deviation 0.309
|
-0.12 scores on a scale
Standard Deviation 0.288
|
-0.11 scores on a scale
Standard Deviation 0.275
|
-0.16 scores on a scale
Standard Deviation 0.349
|
-0.14 scores on a scale
Standard Deviation 0.342
|
SECONDARY outcome
Timeframe: Baseline and Week 3Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of mild, moderate and severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 3. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score =(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=144 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=153 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=131 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=136 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=144 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Mild, Moderate and Severe Vasomotor Symptoms - Week 3 (MITT-VMS)
|
-0.11 scores on a scale
Standard Deviation 0.379
|
-0.20 scores on a scale
Standard Deviation 0.412
|
-0.15 scores on a scale
Standard Deviation 0.350
|
-0.25 scores on a scale
Standard Deviation 0.480
|
-0.24 scores on a scale
Standard Deviation 0.402
|
SECONDARY outcome
Timeframe: Baseline and Week 4Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of mild, moderate and severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 4. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score =(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=142 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=152 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=126 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=134 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=144 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Mild, Moderate and Severe Vasomotor Symptoms - Week 4 (MITT-VMS)
|
-0.19 scores on a scale
Standard Deviation 0.434
|
-0.27 scores on a scale
Standard Deviation 0.507
|
-0.17 scores on a scale
Standard Deviation 0.368
|
-0.31 scores on a scale
Standard Deviation 0.527
|
-0.31 scores on a scale
Standard Deviation 0.540
|
SECONDARY outcome
Timeframe: Baseline and Week 5Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of mild, moderate and severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 5. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score =(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=139 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=147 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=124 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=131 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=143 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Mild, Moderate and Severe Vasomotor Symptoms - Week 5 (MITT-VMS)
|
-0.23 scores on a scale
Standard Deviation 0.441
|
-0.36 scores on a scale
Standard Deviation 0.619
|
-0.24 scores on a scale
Standard Deviation 0.524
|
-0.46 scores on a scale
Standard Deviation 0.680
|
-0.37 scores on a scale
Standard Deviation 0.546
|
SECONDARY outcome
Timeframe: Baseline and Week 6Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of mild, moderate and severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 6. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score =(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=139 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=146 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=123 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=132 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=143 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Mild, Moderate and Severe Vasomotor Symptoms - Week 6 (MITT-VMS)
|
-0.33 scores on a scale
Standard Deviation 0.588
|
-0.46 scores on a scale
Standard Deviation 0.775
|
-0.27 scores on a scale
Standard Deviation 0.548
|
-0.62 scores on a scale
Standard Deviation 0.835
|
-0.42 scores on a scale
Standard Deviation 0.627
|
SECONDARY outcome
Timeframe: Baseline and Week 7Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of mild, moderate and severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 7. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score =(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=139 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=147 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=120 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=130 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=142 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Mild, Moderate and Severe Vasomotor Symptoms - Week 7 (MITT-VMS)
|
-0.42 scores on a scale
Standard Deviation 0.660
|
-0.47 scores on a scale
Standard Deviation 0.773
|
-0.27 scores on a scale
Standard Deviation 0.469
|
-0.65 scores on a scale
Standard Deviation 0.798
|
-0.50 scores on a scale
Standard Deviation 0.687
|
SECONDARY outcome
Timeframe: Baseline and Week 8Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of mild, moderate and severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 8. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score =(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=137 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=147 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=120 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=129 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=140 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Mild, Moderate and Severe Vasomotor Symptoms - Week 8 (MITT-VMS)
|
-0.44 scores on a scale
Standard Deviation 0.701
|
-0.47 scores on a scale
Standard Deviation 0.750
|
-0.33 scores on a scale
Standard Deviation 0.545
|
-0.70 scores on a scale
Standard Deviation 0.858
|
-0.51 scores on a scale
Standard Deviation 0.633
|
SECONDARY outcome
Timeframe: Baseline and Week 9Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of mild, moderate and severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 9. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score =(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=132 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=141 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=119 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=137 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Mild, Moderate and Severe Vasomotor Symptoms - Week 9 (MITT-VMS)
|
-0.51 scores on a scale
Standard Deviation 0.735
|
-0.54 scores on a scale
Standard Deviation 0.780
|
-0.31 scores on a scale
Standard Deviation 0.515
|
-0.78 scores on a scale
Standard Deviation 0.909
|
-0.55 scores on a scale
Standard Deviation 0.708
|
SECONDARY outcome
Timeframe: Baseline and Week 10Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of mild, moderate and severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 10. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score =(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=129 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=140 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=118 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=126 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=133 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Mild, Moderate and Severe Vasomotor Symptoms - Week 10 (MITT-VMS)
|
-0.57 scores on a scale
Standard Deviation 0.785
|
-0.45 scores on a scale
Standard Deviation 0.754
|
-0.35 scores on a scale
Standard Deviation 0.557
|
-0.87 scores on a scale
Standard Deviation 0.970
|
-0.58 scores on a scale
Standard Deviation 0.731
|
SECONDARY outcome
Timeframe: Baseline and Week 11Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of mild, moderate and severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 11. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score =(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=129 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=137 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=118 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=126 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=134 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Mild, Moderate and Severe Vasomotor Symptoms - Week 11 (MITT-VMS)
|
-0.56 scores on a scale
Standard Deviation 0.800
|
-0.50 scores on a scale
Standard Deviation 0.776
|
-0.36 scores on a scale
Standard Deviation 0.543
|
-0.86 scores on a scale
Standard Deviation 0.950
|
-0.67 scores on a scale
Standard Deviation 0.788
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in severity of mild, moderate and severe vasomotor symptoms at Baseline to mild, moderate to severe vasomotor symptoms at Week 12. The baseline was the most recent 7 consecutive days of data prior to randomization. The severity score was derived as follows: mild = 1, moderate = 2, severe = 3. Baseline Weekly Severity Score =(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days). On Treatment Weekly Severity Score = \[(number of mild hot flushes for 7 days) x 1 + (number of moderate hot flushes for 7 days) x 2 + (number of severe hot flushes for 7 days) x 3\] / (total number of mild, moderate and severe hot flushes over 7 days).
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=124 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=135 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=115 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=129 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Severity of Mild, Moderate and Severe Vasomotor Symptoms - Week 12 (MITT-VMS)
|
-0.54 scores on a scale
Standard Deviation 0.761
|
-0.54 scores on a scale
Standard Deviation 0.824
|
-0.39 scores on a scale
Standard Deviation 0.585
|
-0.94 scores on a scale
Standard Deviation 0.986
|
-0.71 scores on a scale
Standard Deviation 0.784
|
SECONDARY outcome
Timeframe: Baseline and Week 1Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of moderate to severe VMS from Baseline to Week 1.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=145 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=154 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=134 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=137 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=149 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 1 (MITT-VMS)
>=50% Reduction
|
15 Participants
|
25 Participants
|
16 Participants
|
15 Participants
|
17 Participants
|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 1 (MITT-VMS)
>=75% Reduction
|
4 Participants
|
5 Participants
|
1 Participants
|
3 Participants
|
4 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 2Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of moderate to severe vasomotor symptoms from Baseline to Week 2.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=145 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=153 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=133 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=133 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=146 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 2 (MITT-VMS)
>=75% Reduction
|
15 Participants
|
20 Participants
|
6 Participants
|
21 Participants
|
12 Participants
|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 2 (MITT-VMS)
>=50% Reduction
|
34 Participants
|
49 Participants
|
35 Participants
|
44 Participants
|
35 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 3Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of moderate to severe vasomotor symptoms from Baseline to Week 3.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=144 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=153 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=131 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=135 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=144 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 3 (MITT-VMS)
>=50% Reduction
|
54 Participants
|
71 Participants
|
42 Participants
|
68 Participants
|
59 Participants
|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 3 (MITT-VMS)
>=75% Reduction
|
21 Participants
|
29 Participants
|
15 Participants
|
38 Participants
|
24 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 4Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of moderate to severe vasomotor symptoms from Baseline to Week 4.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=142 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=152 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=126 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=133 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=144 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 4 (MITT-VMS)
>=50% Reduction
|
74 Participants
|
81 Participants
|
41 Participants
|
82 Participants
|
70 Participants
|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 4 (MITT-VMS)
>=75% Reduction
|
32 Participants
|
45 Participants
|
15 Participants
|
55 Participants
|
34 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 5Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of moderate to severe vasomotor symptoms from Baseline to Week 5.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=139 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=147 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=124 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=130 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=143 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 5 (MITT-VMS)
>=75% Reduction
|
38 Participants
|
54 Participants
|
27 Participants
|
55 Participants
|
47 Participants
|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 5 (MITT-VMS)
>=50% Reduction
|
74 Participants
|
90 Participants
|
55 Participants
|
93 Participants
|
80 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 6Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of moderate to severe vasomotor symptoms from Baseline to Week 6.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=139 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=146 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=123 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=131 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=143 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 6 (MITT-VMS)
>=50% Reduction
|
82 Participants
|
95 Participants
|
55 Participants
|
98 Participants
|
85 Participants
|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 6 (MITT-VMS)
>=75% Reduction
|
47 Participants
|
56 Participants
|
30 Participants
|
68 Participants
|
51 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 7Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of moderate to severe vasomotor symptoms from Baseline to Week 7.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=139 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=147 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=120 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=129 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=142 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 7 (MITT-VMS)
>=50% Reduction
|
88 Participants
|
101 Participants
|
58 Participants
|
96 Participants
|
93 Participants
|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 7 (MITT-VMS)
>=75% Reduction
|
56 Participants
|
58 Participants
|
32 Participants
|
71 Participants
|
63 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 8Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of moderate to severe vasomotor symptoms from Baseline to Week 8.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=137 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=147 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=120 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=129 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=140 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 8 (MITT-VMS)
>=50% Reduction
|
90 Participants
|
100 Participants
|
60 Participants
|
102 Participants
|
98 Participants
|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 8 (MITT-VMS)
>=75% Reduction
|
59 Participants
|
62 Participants
|
37 Participants
|
78 Participants
|
64 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 9Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of moderate to severe vasomotor symptoms from Baseline to Week 9.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=132 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=141 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=119 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=137 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 9 (MITT-VMS)
>=75% Reduction
|
63 Participants
|
63 Participants
|
35 Participants
|
72 Participants
|
73 Participants
|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 9 (MITT-VMS)
>=50% Reduction
|
92 Participants
|
101 Participants
|
63 Participants
|
98 Participants
|
107 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 10Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of moderate to severe vasomotor symptoms from Baseline to Week 10.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=129 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=140 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=118 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=126 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=133 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 10 (MITT-VMS)
>=50% Reduction
|
100 Participants
|
101 Participants
|
68 Participants
|
95 Participants
|
102 Participants
|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 10 (MITT-VMS)
>=75% Reduction
|
62 Participants
|
64 Participants
|
37 Participants
|
78 Participants
|
69 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 11Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of moderate to severe vasomotor symptoms from Baseline to Week 11.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=129 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=137 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=118 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=126 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=134 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 11 (MITT-VMS)
>=50% Reduction
|
97 Participants
|
104 Participants
|
59 Participants
|
95 Participants
|
105 Participants
|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 11 (MITT-VMS)
>=75% Reduction
|
65 Participants
|
68 Participants
|
34 Participants
|
79 Participants
|
74 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of moderate to severe vasomotor symptoms from Baseline to Week 12.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=124 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=135 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=115 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=129 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 12 (MITT-VMS)
>=50% Reduction
|
94 Participants
|
99 Participants
|
67 Participants
|
98 Participants
|
104 Participants
|
|
Reduction of Frequency of Moderate to Severe Vasomotor Symptoms - Week 12 (MITT-VMS)
>=75% Reduction
|
66 Participants
|
68 Participants
|
37 Participants
|
84 Participants
|
75 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 1Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 1.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=145 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=154 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=134 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=138 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=149 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 1 - (MITT-VMS)
>=50% Reduction
|
12 Participants
|
19 Participants
|
10 Participants
|
14 Participants
|
10 Participants
|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 1 - (MITT-VMS)
>=75% Reduction
|
1 Participants
|
4 Participants
|
1 Participants
|
2 Participants
|
2 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 2Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 2.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=145 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=153 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=133 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=134 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=146 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 2 - (MITT-VMS)
>=50% Reduction
|
30 Participants
|
39 Participants
|
21 Participants
|
36 Participants
|
24 Participants
|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 2 - (MITT-VMS)
>=75% Reduction
|
9 Participants
|
17 Participants
|
4 Participants
|
15 Participants
|
7 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 3Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 3.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=144 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=153 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=131 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=136 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=144 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 3 - (MITT-VMS)
>=75% Reduction
|
15 Participants
|
22 Participants
|
6 Participants
|
33 Participants
|
14 Participants
|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 3 - (MITT-VMS)
>=50% Reduction
|
50 Participants
|
61 Participants
|
33 Participants
|
63 Participants
|
49 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 4Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 4.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=142 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=152 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=126 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=134 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=144 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 4 - (MITT-VMS)
>=50% Reduction
|
65 Participants
|
73 Participants
|
35 Participants
|
80 Participants
|
62 Participants
|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 4 - (MITT-VMS)
>=75% Reduction
|
24 Participants
|
33 Participants
|
6 Participants
|
44 Participants
|
28 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 5Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 5.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=139 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=147 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=124 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=131 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=143 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 5 - (MITT-VMS)
>=50% Reduction
|
69 Participants
|
82 Participants
|
47 Participants
|
86 Participants
|
72 Participants
|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 5 - (MITT-VMS)
>=75% Reduction
|
27 Participants
|
37 Participants
|
13 Participants
|
48 Participants
|
34 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 6Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 6.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=139 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=146 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=123 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=132 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=143 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 6 - (MITT-VMS)
>=75% Reduction
|
39 Participants
|
43 Participants
|
16 Participants
|
61 Participants
|
39 Participants
|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 6 - (MITT-VMS)
>=50% Reduction
|
76 Participants
|
83 Participants
|
52 Participants
|
92 Participants
|
78 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 7Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 7.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=139 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=147 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=120 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=130 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=142 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 7 - (MITT-VMS)
>=50% Reduction
|
81 Participants
|
95 Participants
|
49 Participants
|
93 Participants
|
87 Participants
|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 7 - (MITT-VMS)
>=75% Reduction
|
44 Participants
|
47 Participants
|
16 Participants
|
63 Participants
|
46 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 8Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 8.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=137 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=147 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=120 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=129 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=140 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 8 - (MITT-VMS)
>=50% Reduction
|
90 Participants
|
93 Participants
|
54 Participants
|
98 Participants
|
85 Participants
|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 8 - (MITT-VMS)
>=75% Reduction
|
45 Participants
|
51 Participants
|
20 Participants
|
64 Participants
|
53 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 9Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 9.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=132 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=141 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=119 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=137 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 9 - (MITT-VMS)
>=75% Reduction
|
54 Participants
|
56 Participants
|
22 Participants
|
69 Participants
|
63 Participants
|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 9 - (MITT-VMS)
>=50% Reduction
|
91 Participants
|
94 Participants
|
58 Participants
|
95 Participants
|
95 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 10Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 10.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=129 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=140 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=118 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=126 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=133 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 10 - (MITT-VMS)
>=75% Reduction
|
57 Participants
|
57 Participants
|
23 Participants
|
73 Participants
|
60 Participants
|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 10 - (MITT-VMS)
>=50% Reduction
|
92 Participants
|
93 Participants
|
54 Participants
|
93 Participants
|
94 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 11Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 11.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=129 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=137 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=118 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=126 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=134 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 11 - (MITT-VMS)
>=50% Reduction
|
94 Participants
|
95 Participants
|
55 Participants
|
94 Participants
|
97 Participants
|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 11 - (MITT-VMS)
>=75% Reduction
|
52 Participants
|
62 Participants
|
26 Participants
|
71 Participants
|
64 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Number of Subjects with \>=50%, and separately, \>=75% reduction in frequency of mild, moderate and severe vasomotor symptoms from Baseline to Week 12.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=124 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=135 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=115 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=129 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 12 - (MITT-VMS)
>=75% Reduction
|
50 Participants
|
58 Participants
|
32 Participants
|
73 Participants
|
64 Participants
|
|
Reduction of Frequency of Mild, Moderate and Severe Vasomotor Symptoms - Week 12 - (MITT-VMS)
>=50% Reduction
|
90 Participants
|
95 Participants
|
55 Participants
|
97 Participants
|
94 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 4Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
The number and percentage of subjects for each possible response to the CGI at Week 4. The CGI score is a seven point scale where subjects were asked to rate the total improvement, whether or not in her judgment it was due entirely to drug treatment, compared to her condition at admission to the study. Scale: Very much improved, Much improved, Minimally improved, No change, Minimally worse, Much worse, Very much worse. Results for the top two responses (Very Much Improved and Much Improved) and No Change or Worsening (Minimally worse, Much worse, Very much worse) were combined for each group and active treatment groups compare to placebo.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=144 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=148 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=125 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=136 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=141 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Clinical Global Impression (CGI) - Week 4 (MITT-VMS)
(Very) Much Improved
|
72 Participants
|
75 Participants
|
41 Participants
|
86 Participants
|
71 Participants
|
|
Clinical Global Impression (CGI) - Week 4 (MITT-VMS)
No Change or Worse
|
23 Participants
|
22 Participants
|
35 Participants
|
13 Participants
|
21 Participants
|
|
Clinical Global Impression (CGI) - Week 4 (MITT-VMS)
Minimally Improved
|
49 Participants
|
51 Participants
|
49 Participants
|
37 Participants
|
49 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 4Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of moderate to severe vasomotor symptoms from Baseline to Week 4 for the respective CGI category. The CGI score is a seven point scale where subjects were asked to rate the total improvement, whether or not in her judgment it was due entirely to drug treatment, compared to her condition at admission to the study. Scale: Very much improved, Much improved, Minimally improved, No change, Minimally worse, Much worse, Very much worse. Results for the top two responses (Very Much Improved and Much Improved) and No Change or Worsening (Minimally worse, Much worse, Very much worse) were combined for each group and active treatment groups compare to placebo.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=144 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=148 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=125 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=136 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=141 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Mean Change in Frequency of Moderate to Severe VMS for the Respective CGI Category - Week 4 (MITT-VMS)
(Very) Much Improved
|
-46.2 weekly hot flushes
Standard Deviation 31.23
|
-55.7 weekly hot flushes
Standard Deviation 25.69
|
-47.0 weekly hot flushes
Standard Deviation 24.17
|
-52.5 weekly hot flushes
Standard Deviation 27.28
|
-48.6 weekly hot flushes
Standard Deviation 28.87
|
|
Mean Change in Frequency of Moderate to Severe VMS for the Respective CGI Category - Week 4 (MITT-VMS)
Minimally Improved
|
-29.2 weekly hot flushes
Standard Deviation 23.26
|
-28.9 weekly hot flushes
Standard Deviation 26.08
|
-26.8 weekly hot flushes
Standard Deviation 17.68
|
-24.1 weekly hot flushes
Standard Deviation 23.87
|
-25.9 weekly hot flushes
Standard Deviation 21.43
|
|
Mean Change in Frequency of Moderate to Severe VMS for the Respective CGI Category - Week 4 (MITT-VMS)
No Change or Worse
|
-2.7 weekly hot flushes
Standard Deviation 16.22
|
-5.3 weekly hot flushes
Standard Deviation 21.97
|
-5.3 weekly hot flushes
Standard Deviation 13.68
|
-6.5 weekly hot flushes
Standard Deviation 23.08
|
-6.6 weekly hot flushes
Standard Deviation 16.39
|
SECONDARY outcome
Timeframe: Baseline and Week 8Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
The number and percentage of subjects for each possible response to the CGI at Week 8. The CGI score is a seven point scale where subjects were asked to rate the total improvement, whether or not in her judgment it was due entirely to drug treatment, compared to her condition at admission to the study. Scale: Very much improved, Much improved, Minimally improved, No change, Minimally worse, Much worse, Very much worse. Results for the top two responses (Very Much Improved and Much Improved) and No Change or Worsening (Minimally worse, Much worse, Very much worse) were combined for each group and active treatment groups compare to placebo.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=134 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=141 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=117 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=130 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=139 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Clinical Global Impression (CGI) - Week 8 (MITT-VMS)
(Very) Much Improved
|
98 Participants
|
93 Participants
|
62 Participants
|
101 Participants
|
103 Participants
|
|
Clinical Global Impression (CGI) - Week 8 (MITT-VMS)
Minimally Improved
|
23 Participants
|
35 Participants
|
25 Participants
|
23 Participants
|
24 Participants
|
|
Clinical Global Impression (CGI) - Week 8 (MITT-VMS)
No Change or Worse
|
13 Participants
|
13 Participants
|
30 Participants
|
6 Participants
|
12 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 8Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of moderate to severe vasomotor symptoms from Baseline to Week 8 for the respective CGI category. The CGI score is a seven point scale where subjects were asked to rate the total improvement, whether or not in her judgment it was due entirely to drug treatment, compared to her condition at admission to the study. Scale: Very much improved, Much improved, Minimally improved, No change, Minimally worse, Much worse, Very much worse. Results for the top two responses (Very Much Improved and Much Improved) and No Change or Worsening (Minimally worse, Much worse, Very much worse) were combined for each group and active treatment groups compare to placebo.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=134 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=141 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=117 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=130 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=139 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Mean Change in Frequency of Moderate to Severe VMS for the Respective CGI Category - Week 8 (MITT-VMS)
(Very) Much Improved
|
-55.4 weekly hot flushes
Standard Deviation 29.06
|
-57.8 weekly hot flushes
Standard Deviation 30.38
|
-52.6 weekly hot flushes
Standard Deviation 24.62
|
-60.8 weekly hot flushes
Standard Deviation 28.49
|
-55.1 weekly hot flushes
Standard Deviation 29.27
|
|
Mean Change in Frequency of Moderate to Severe VMS for the Respective CGI Category - Week 8 (MITT-VMS)
Minimally Improved
|
-27.2 weekly hot flushes
Standard Deviation 22.79
|
-36.8 weekly hot flushes
Standard Deviation 24.81
|
-27.0 weekly hot flushes
Standard Deviation 13.54
|
-28.7 weekly hot flushes
Standard Deviation 18.93
|
-27.3 weekly hot flushes
Standard Deviation 25.22
|
|
Mean Change in Frequency of Moderate to Severe VMS for the Respective CGI Category - Week 8 (MITT-VMS)
No Change or Worse
|
-1.6 weekly hot flushes
Standard Deviation 19.93
|
-7.4 weekly hot flushes
Standard Deviation 21.48
|
-7.1 weekly hot flushes
Standard Deviation 21.46
|
-0.2 weekly hot flushes
Standard Deviation 28.80
|
-15.2 weekly hot flushes
Standard Deviation 13.41
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
The number and percentage of subjects for each possible response to the CGI at Week 12. The CGI score is a seven point scale where subjects were asked to rate the total improvement, whether or not in her judgment it was due entirely to drug treatment, compared to her condition at admission to the study. Scale: Very much improved, Much improved, Minimally improved, No change, Minimally worse, Much worse, Very much worse. Results for the top two responses (Very Much Improved and Much Improved) and No Change or Worsening (Minimally worse, Much worse, Very much worse) were combined for each group and active treatment groups compare to placebo.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=131 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=139 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=116 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=123 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=133 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Clinical Global Impression (CGI) - Week 12 (MITT-VMS)
Minimally Improved
|
22 Participants
|
24 Participants
|
26 Participants
|
17 Participants
|
29 Participants
|
|
Clinical Global Impression (CGI) - Week 12 (MITT-VMS)
No Change or Worse
|
7 Participants
|
14 Participants
|
28 Participants
|
5 Participants
|
7 Participants
|
|
Clinical Global Impression (CGI) - Week 12 (MITT-VMS)
(Very) Much Improved
|
102 Participants
|
101 Participants
|
62 Participants
|
101 Participants
|
97 Participants
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Mean change in frequency of moderate to severe vasomotor symptoms from Baseline to Week 12 for the respective CGI category. The CGI score is a seven point scale where subjects were asked to rate the total improvement, whether or not in her judgment it was due entirely to drug treatment, compared to her condition at admission to the study. Scale: Very much improved, Much improved, Minimally improved, No change, Minimally worse, Much worse, Very much worse. Results for the top two responses (Very Much Improved and Much Improved) and No Change or Worsening (Minimally worse, Much worse, Very much worse) were combined for each group and active treatment groups compare to placebo.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=131 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=139 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=116 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=123 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=133 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Mean Change in Frequency of Moderate to Severe VMS for the Respective CGI Category - Week 12 (MITT-VMS)
Minimally Improved
|
-28.8 weekly hot flushes
Standard Deviation 21.99
|
-40.6 weekly hot flushes
Standard Deviation 37.36
|
-35.7 weekly hot flushes
Standard Deviation 19.55
|
-35.9 weekly hot flushes
Standard Deviation 24.78
|
-34.9 weekly hot flushes
Standard Deviation 40.36
|
|
Mean Change in Frequency of Moderate to Severe VMS for the Respective CGI Category - Week 12 (MITT-VMS)
(Very) Much Improved
|
-58.2 weekly hot flushes
Standard Deviation 29.42
|
-59.9 weekly hot flushes
Standard Deviation 28.01
|
-56.2 weekly hot flushes
Standard Deviation 26.50
|
-58.8 weekly hot flushes
Standard Deviation 30.71
|
-60.0 weekly hot flushes
Standard Deviation 28.37
|
|
Mean Change in Frequency of Moderate to Severe VMS for the Respective CGI Category - Week 12 (MITT-VMS)
No Change or Worse
|
-8.6 weekly hot flushes
Standard Deviation 18.42
|
-8.3 weekly hot flushes
Standard Deviation 31.84
|
-9.2 weekly hot flushes
Standard Deviation 16.77
|
-30.7 weekly hot flushes
Standard Deviation 32.89
|
-38.8 weekly hot flushes
Standard Deviation 18.99
|
SECONDARY outcome
Timeframe: Cycle 1 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
No bleeding was defined as the absence of bleeding. Cumulative rates for no bleeding was defined as the percentage of women who reported consecutive cycles of no bleeding for a given cycle of time.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=268 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=278 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=299 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects Without Bleeding for Consecutive Cycles
|
263 Participants
|
239 Participants
|
82 Participants
|
204 Participants
|
251 Participants
|
SECONDARY outcome
Timeframe: Cycle 2 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
No bleeding was defined as the absence of bleeding. Cumulative rates for no bleeding was defined as the percentage of women who reported consecutive cycles of no bleeding for a given cycle of time.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=268 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=278 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=299 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects Without Bleeding for Consecutive Cycles
|
265 Participants
|
244 Participants
|
84 Participants
|
209 Participants
|
256 Participants
|
SECONDARY outcome
Timeframe: Cycle 3 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
No bleeding was defined as the absence of bleeding. Cumulative rates for no bleeding was defined as the percentage of women who reported consecutive cycles of no bleeding for a given cycle of time.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=268 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=278 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=299 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects Without Bleeding for Consecutive Cycles
|
267 Participants
|
246 Participants
|
85 Participants
|
214 Participants
|
258 Participants
|
SECONDARY outcome
Timeframe: Cycle 4 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
No bleeding was defined as the absence of bleeding. Cumulative rates for no bleeding was defined as the percentage of women who reported consecutive cycles of no bleeding for a given cycle of time.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=268 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=278 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=299 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects Without Bleeding for Consecutive Cycles
|
273 Participants
|
253 Participants
|
86 Participants
|
217 Participants
|
261 Participants
|
SECONDARY outcome
Timeframe: Cycle 5 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
No bleeding was defined as the absence of bleeding. Cumulative rates for no bleeding was defined as the percentage of women who reported consecutive cycles of no bleeding for a given cycle of time.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=268 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=278 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=299 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects Without Bleeding for Consecutive Cycles
|
278 Participants
|
253 Participants
|
86 Participants
|
224 Participants
|
265 Participants
|
SECONDARY outcome
Timeframe: Cycle 6 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
No bleeding was defined as the absence of bleeding. Cumulative rates for no bleeding was defined as the percentage of women who reported consecutive cycles of no bleeding for a given cycle of time.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=268 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=278 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=299 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects Without Bleeding for Consecutive Cycles
|
280 Participants
|
256 Participants
|
86 Participants
|
227 Participants
|
268 Participants
|
SECONDARY outcome
Timeframe: Cycle 7 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
No bleeding was defined as the absence of bleeding. Cumulative rates for no bleeding was defined as the percentage of women who reported consecutive cycles of no bleeding for a given cycle of time.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=268 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=278 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=299 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects Without Bleeding for Consecutive Cycles
|
282 Participants
|
256 Participants
|
87 Participants
|
237 Participants
|
271 Participants
|
SECONDARY outcome
Timeframe: Cycle 8 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
No bleeding was defined as the absence of bleeding. Cumulative rates for no bleeding was defined as the percentage of women who reported consecutive cycles of no bleeding for a given cycle of time.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=268 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=278 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=299 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects Without Bleeding for Consecutive Cycles
|
285 Participants
|
258 Participants
|
88 Participants
|
242 Participants
|
276 Participants
|
SECONDARY outcome
Timeframe: Cycle 9 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
No bleeding was defined as the absence of bleeding. Cumulative rates for no bleeding was defined as the percentage of women who reported consecutive cycles of no bleeding for a given cycle of time.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=268 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=278 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=299 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects Without Bleeding for Consecutive Cycles
|
288 Participants
|
259 Participants
|
88 Participants
|
245 Participants
|
279 Participants
|
SECONDARY outcome
Timeframe: Cycle 10 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
No bleeding was defined as the absence of bleeding. Cumulative rates for no bleeding was defined as the percentage of women who reported consecutive cycles of no bleeding for a given cycle of time.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=268 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=278 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=299 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects Without Bleeding for Consecutive Cycles
|
292 Participants
|
261 Participants
|
88 Participants
|
248 Participants
|
281 Participants
|
SECONDARY outcome
Timeframe: Cycle 11 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
No bleeding was defined as the absence of bleeding. Cumulative rates for no bleeding was defined as the percentage of women who reported consecutive cycles of no bleeding for a given cycle of time.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=302 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=266 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=276 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=297 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects Without Bleeding for Consecutive Cycles
|
294 Participants
|
261 Participants
|
88 Participants
|
251 Participants
|
284 Participants
|
SECONDARY outcome
Timeframe: Cycle 12 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
No bleeding was defined as the absence of bleeding. Cumulative rates for no bleeding was defined as the percentage of women who reported consecutive cycles of no bleeding for a given cycle of time.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=302 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=265 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=276 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=297 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects Without Bleeding for Consecutive Cycles
|
295 Participants
|
260 Participants
|
88 Participants
|
260 Participants
|
284 Participants
|
SECONDARY outcome
Timeframe: The 13th CyclePopulation: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
No bleeding was defined as the absence of bleeding. Cumulative rates for no bleeding was defined as the percentage of women who reported consecutive cycles of no bleeding for a given cycle of time.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=302 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=264 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=276 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=294 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects Without Bleeding for Consecutive Cycles
|
296 Participants
|
261 Participants
|
89 Participants
|
268 Participants
|
287 Participants
|
SECONDARY outcome
Timeframe: Cycle 1 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
Cumulative amenorrhea is defined as the absence of bleeding or spotting for a cumulative period. Cumulative rates of amenorrhea were defined as the percentage of women who reported consecutive cycles of amenorrhea for a given cycle of time. Within each treatment arm, the percentage of subjects with cumulative amenorrhea from Cycle 1 to 13 was calculated and compared between active and placebo treatments.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=268 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=278 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=299 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects With Cumulative Amenorrhea From Cycle 1 to 13
|
207 Participants
|
196 Participants
|
71 Participants
|
156 Participants
|
202 Participants
|
SECONDARY outcome
Timeframe: Cycle 2 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
Cumulative amenorrhea is defined as the absence of bleeding or spotting for a cumulative period. Cumulative rates of amenorrhea were defined as the percentage of women who reported consecutive cycles of amenorrhea for a given cycle of time. Within each treatment arm, the percentage of subjects with cumulative amenorrhea from Cycle 2 to 13 was calculated and compared between active and placebo treatments.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=268 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=278 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=299 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects With Cumulative Amenorrhea From Cycle 2 to 13
|
215 Participants
|
212 Participants
|
74 Participants
|
166 Participants
|
220 Participants
|
SECONDARY outcome
Timeframe: Cycle 3 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
Cumulative amenorrhea is defined as the absence of bleeding or spotting for a cumulative period. Cumulative rates of amenorrhea were defined as the percentage of women who reported consecutive cycles of amenorrhea for a given cycle of time. Within each treatment arm, the percentage of subjects with cumulative amenorrhea from Cycle 3 to 13 was calculated and compared between active and placebo treatments.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=268 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=278 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=299 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects With Cumulative Amenorrhea From Cycle 3 to 13
|
225 Participants
|
218 Participants
|
77 Participants
|
174 Participants
|
227 Participants
|
SECONDARY outcome
Timeframe: Cycle 4 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
Cumulative amenorrhea is defined as the absence of bleeding or spotting for a cumulative period. Cumulative rates of amenorrhea were defined as the percentage of women who reported consecutive cycles of amenorrhea for a given cycle of time. Within each treatment arm, the percentage of subjects with cumulative amenorrhea from Cycle 4 to 13 was calculated and compared between active and placebo treatments.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=268 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=278 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=299 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects With Cumulative Amenorrhea From Cycle 4 to 13
|
233 Participants
|
229 Participants
|
80 Participants
|
177 Participants
|
236 Participants
|
SECONDARY outcome
Timeframe: Cycle 5 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
Cumulative amenorrhea is defined as the absence of bleeding or spotting for a cumulative period. Cumulative rates of amenorrhea were defined as the percentage of women who reported consecutive cycles of amenorrhea for a given cycle of time. Within each treatment arm, the percentage of subjects with cumulative amenorrhea from Cycle 5 to 13 was calculated and compared between active and placebo treatments.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=268 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=278 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=299 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects With Cumulative Amenorrhea From Cycle 5 to 13
|
240 Participants
|
234 Participants
|
80 Participants
|
183 Participants
|
244 Participants
|
SECONDARY outcome
Timeframe: Cycle 6 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
Cumulative amenorrhea is defined as the absence of bleeding or spotting for a cumulative period. Cumulative rates of amenorrhea were defined as the percentage of women who reported consecutive cycles of amenorrhea for a given cycle of time. Within each treatment arm, the percentage of subjects with cumulative amenorrhea from Cycle 6 to 13 was calculated and compared between active and placebo treatments.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=268 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=278 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=299 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects With Cumulative Amenorrhea From Cycle 6 to 13
|
249 Participants
|
236 Participants
|
80 Participants
|
186 Participants
|
250 Participants
|
SECONDARY outcome
Timeframe: Cycle 7 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
Cumulative amenorrhea is defined as the absence of bleeding or spotting for a cumulative period. Cumulative rates of amenorrhea were defined as the percentage of women who reported consecutive cycles of amenorrhea for a given cycle of time. Within each treatment arm, the percentage of subjects with cumulative amenorrhea from Cycle 7 to 13 was calculated and compared between active and placebo treatments.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=268 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=278 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=299 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects With Cumulative Amenorrhea From Cycle 7 to 13
|
255 Participants
|
238 Participants
|
82 Participants
|
200 Participants
|
253 Participants
|
SECONDARY outcome
Timeframe: Cycle 8 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
Cumulative amenorrhea is defined as the absence of bleeding or spotting for a cumulative period. Cumulative rates of amenorrhea were defined as the percentage of women who reported consecutive cycles of amenorrhea for a given cycle of time. Within each treatment arm, the percentage of subjects with cumulative amenorrhea from Cycle 8 to 13 was calculated and compared between active and placebo treatments.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=268 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=278 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=299 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects With Cumulative Amenorrhea From Cycle 8 to 13
|
262 Participants
|
242 Participants
|
84 Participants
|
209 Participants
|
262 Participants
|
SECONDARY outcome
Timeframe: Cycle 9 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
Cumulative amenorrhea is defined as the absence of bleeding or spotting for a cumulative period. Cumulative rates of amenorrhea were defined as the percentage of women who reported consecutive cycles of amenorrhea for a given cycle of time. Within each treatment arm, the percentage of subjects with cumulative amenorrhea from Cycle 9 to 13 was calculated and compared between active and placebo treatments.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=268 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=278 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=299 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects With Cumulative Amenorrhea From Cycle 9 to 13
|
266 Participants
|
246 Participants
|
84 Participants
|
214 Participants
|
267 Participants
|
SECONDARY outcome
Timeframe: Cycle 10 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
Cumulative amenorrhea is defined as the absence of bleeding or spotting for a cumulative period. Cumulative rates of amenorrhea were defined as the percentage of women who reported consecutive cycles of amenorrhea for a given cycle of time. Within each treatment arm, the percentage of subjects with cumulative amenorrhea from Cycle 10 to 13 was calculated and compared between active and placebo treatments.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=268 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=278 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=299 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects With Cumulative Amenorrhea From Cycle 10 to 13
|
273 Participants
|
248 Participants
|
85 Participants
|
222 Participants
|
271 Participants
|
SECONDARY outcome
Timeframe: Cycle 11 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
Cumulative amenorrhea is defined as the absence of bleeding or spotting for a cumulative period. Cumulative rates of amenorrhea were defined as the percentage of women who reported consecutive cycles of amenorrhea for a given cycle of time. Within each treatment arm, the percentage of subjects with cumulative amenorrhea from Cycle 11 to 13 was calculated and compared between active and placebo treatments.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=302 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=266 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=276 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=297 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects With Cumulative Amenorrhea From Cycle 11 to 13
|
277 Participants
|
249 Participants
|
85 Participants
|
231 Participants
|
275 Participants
|
SECONDARY outcome
Timeframe: Cycle 12 to 13Population: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
Cumulative amenorrhea is defined as the absence of bleeding or spotting for a cumulative period. Cumulative rates of amenorrhea were defined as the percentage of women who reported consecutive cycles of amenorrhea for a given cycle of time. Within each treatment arm, the percentage of subjects with cumulative amenorrhea from Cycle 12 to 13 was calculated and compared between active and placebo treatments.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=302 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=265 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=276 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=297 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects With Cumulative Amenorrhea From Cycle 12 to 13
|
278 Participants
|
252 Participants
|
86 Participants
|
238 Participants
|
278 Participants
|
SECONDARY outcome
Timeframe: The 13th CyclePopulation: Subjects who received study drug for at least 1 complete 28-day cycle (at least 23 days in length); subjects who reported bleeding days during a partial cycle are also included.
Cumulative amenorrhea is defined as the absence of bleeding or spotting for a cumulative period. Cumulative rates of amenorrhea were defined as the percentage of women who reported consecutive cycles of amenorrhea for a given cycle of time. Within each treatment arm, the percentage of subjects with cumulative amenorrhea from the 13th Cycle was calculated and compared between active and placebo treatments.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=302 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=264 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=90 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=276 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=294 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Subjects With Cumulative Amenorrhea From the 13th Cycle
|
283 Participants
|
254 Participants
|
88 Participants
|
249 Participants
|
282 Participants
|
SECONDARY outcome
Timeframe: Trimester 1Population: Subjects who had taken at least one dose (2 capsules) of IP and had at least one bleeding/spotting diary entry for Trimester 1. Subjects who reported bleeding/spotting diary only for partial trimester are also included.
Summary of subject incidence with spotting per trimester as recorded in a daily diary. A trimester is defined as every 90 days since Day 1.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=334 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=307 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=103 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=312 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=329 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Subject Incidence With Spotting - Trimester 1 (Safety Pop.)
|
68 Participants
|
58 Participants
|
10 Participants
|
90 Participants
|
74 Participants
|
SECONDARY outcome
Timeframe: Trimester 2Population: Subjects who had taken at least one dose (2 capsules) of IP and had at least one bleeding/spotting diary entry for Trimester 2. Subjects who reported bleeding/spotting diary only for partial trimester are also included.
Summary of subject incidence with spotting per trimester as recorded in a daily diary. A trimester is defined as every 90 days since Day 1.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=325 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=302 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=98 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=309 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=323 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Subject Incidence With Spotting - Trimester 2 (Safety Pop.)
|
48 Participants
|
24 Participants
|
4 Participants
|
76 Participants
|
40 Participants
|
SECONDARY outcome
Timeframe: Trimester 3Population: Subjects who had taken at least one dose (2 capsules) of IP and had at least one bleeding/spotting diary entry for Trimester 3. Subjects who reported bleeding/spotting diary only for partial trimester are also included.
Summary of subject incidence with spotting per trimester as recorded in a daily diary. A trimester is defined as every 90 days since Day 1.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=320 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=288 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=97 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=298 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=311 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Subject Incidence With Spotting - Trimester 3 (Safety Pop.)
|
29 Participants
|
18 Participants
|
2 Participants
|
54 Participants
|
33 Participants
|
SECONDARY outcome
Timeframe: Trimester 4Population: Subjects who had taken at least one dose (2 capsules) of IP and had at least one bleeding/spotting diary entry for Trimester 4. Subjects who reported bleeding/spotting diary only for partial trimester are also included.
Summary of subject incidence with spotting per trimester as recorded in a daily diary. A trimester is defined as every 90 days since Day 1.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=308 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=276 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=282 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Subject Incidence With Spotting - Trimester 4 (Safety Pop.)
|
27 Participants
|
18 Participants
|
4 Participants
|
47 Participants
|
21 Participants
|
SECONDARY outcome
Timeframe: Trimester 1Population: Subjects who had taken at least one dose (2 capsules) of IP and had at least one bleeding/spotting diary entry for Trimester 1. Subjects who reported bleeding/spotting diary only for partial trimester are also included.
Summary of the number of days with spotting per trimester as recorded in a daily diary. A trimester is defined as every 90 days since Day 1.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=334 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=307 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=103 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=312 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=329 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Days With Spotting - Trimester 1 (Safety Pop.)
|
1.3 Days
Standard Deviation 5.08
|
0.8 Days
Standard Deviation 2.29
|
0.6 Days
Standard Deviation 2.63
|
3.0 Days
Standard Deviation 8.81
|
1.7 Days
Standard Deviation 6.05
|
SECONDARY outcome
Timeframe: Trimester 2Population: Subjects who had taken at least one dose (2 capsules) of IP and had at least one bleeding/spotting diary entry for Trimester 2. Subjects who reported bleeding/spotting diary only for partial trimester are also included.
Summary of the number of days with spotting per trimester as recorded in a daily diary. A trimester is defined as every 90 days since Day 1.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=325 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=302 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=98 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=309 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=323 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Days With Spotting - Trimester 2 (Safety Pop.)
|
1.5 Days
Standard Deviation 9.16
|
0.7 Days
Standard Deviation 4.30
|
0.1 Days
Standard Deviation 0.74
|
2.9 Days
Standard Deviation 8.63
|
0.9 Days
Standard Deviation 3.85
|
SECONDARY outcome
Timeframe: Trimester 3Population: Subjects who had taken at least one dose (2 capsules) of IP and had at least one bleeding/spotting diary entry for Trimester 3. Subjects who reported bleeding/spotting diary only for partial trimester are also included.
Summary of the number of days with spotting per trimester as recorded in a daily diary. A trimester is defined as every 90 days since Day 1.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=320 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=288 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=97 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=298 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=311 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Days With Spotting - Trimester 3 (Safety Pop.)
|
0.9 Days
Standard Deviation 6.04
|
0.3 Days
Standard Deviation 1.90
|
0.0 Days
Standard Deviation 0.14
|
2.5 Days
Standard Deviation 8.28
|
0.7 Days
Standard Deviation 2.55
|
SECONDARY outcome
Timeframe: Trimester 4Population: Subjects who had taken at least one dose (2 capsules) of IP and had at least one bleeding/spotting diary entry for Trimester 4. Subjects who reported bleeding/spotting diary only for partial trimester are also included.
Summary of the number of days with spotting per trimester as recorded in a daily diary. A trimester is defined as every 90 days since Day 1.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=308 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=276 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=282 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Days With Spotting - Trimester 4 (Safety Pop.)
|
0.8 Days
Standard Deviation 5.75
|
0.3 Days
Standard Deviation 1.17
|
0.1 Days
Standard Deviation 0.67
|
1.9 Days
Standard Deviation 7.59
|
0.5 Days
Standard Deviation 3.36
|
SECONDARY outcome
Timeframe: Trimester 1Population: Subjects who had taken at least one dose (2 capsules) of IP and had at least one bleeding/spotting diary entry for Trimester 1. Subjects who reported bleeding/spotting diary only for partial trimester are also included.
Summary of subject incidence with bleeding per trimester as recorded in a daily diary. A trimester is defined as every 90 days since Day 1.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=334 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=307 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=103 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=312 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=329 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Subject Incidence With Bleeding - Trimester 1 (Safety Pop.)
|
25 Participants
|
24 Participants
|
4 Participants
|
48 Participants
|
29 Participants
|
SECONDARY outcome
Timeframe: Trimester 2Population: Subjects who had taken at least one dose (2 capsules) of IP and had at least one bleeding/spotting diary entry for Trimester 2. Subjects who reported bleeding/spotting diary only for partial trimester are also included.
Summary of subject incidence with bleeding per trimester as recorded in a daily diary. A trimester is defined as every 90 days since Day 1.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=325 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=302 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=98 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=309 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=323 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Subject Incidence With Bleeding - Trimester 2 (Safety Pop.)
|
19 Participants
|
5 Participants
|
2 Participants
|
45 Participants
|
23 Participants
|
SECONDARY outcome
Timeframe: Trimester 3Population: Subjects who had taken at least one dose (2 capsules) of IP and had at least one bleeding/spotting diary entry for Trimester 3. Subjects who reported bleeding/spotting diary only for partial trimester are also included.
Summary of subject incidence with bleeding per trimester as recorded in a daily diary. A trimester is defined as every 90 days since Day 1.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=320 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=288 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=97 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=298 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=311 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Subject Incidence With Bleeding - Trimester 3 (Safety Pop.)
|
16 Participants
|
7 Participants
|
1 Participants
|
25 Participants
|
21 Participants
|
SECONDARY outcome
Timeframe: Trimester 4Population: Subjects who had taken at least one dose (2 capsules) of IP and had at least one bleeding/spotting diary entry for Trimester 4. Subjects who reported bleeding/spotting diary only for partial trimester are also included.
Summary of subject incidence with bleeding per trimester as recorded in a daily diary. A trimester is defined as every 90 days since Day 1.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=308 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=276 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=282 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Subject Incidence With Bleeding - Trimester 4 (Safety Pop.)
|
9 Participants
|
5 Participants
|
2 Participants
|
27 Participants
|
16 Participants
|
SECONDARY outcome
Timeframe: Trimester 1Population: Subjects who had taken at least one dose (2 capsules) of IP and had at least one bleeding/spotting diary entry for Trimester 1. Subjects who reported bleeding/spotting diary only for partial trimester are also included.
Summary of the number of days with bleeding per trimester as recorded in a daily diary. A trimester is defined as every 90 days since Day 1.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=334 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=307 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=103 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=312 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=329 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Days With Bleeding - Trimester 1 (Safety Pop.)
|
0.5 Days
Standard Deviation 2.24
|
0.4 Days
Standard Deviation 1.79
|
0.2 Days
Standard Deviation 1.01
|
1.2 Days
Standard Deviation 5.22
|
0.5 Days
Standard Deviation 2.21
|
SECONDARY outcome
Timeframe: Trimester 2Population: Subjects who had taken at least one dose (2 capsules) of IP and had at least one bleeding/spotting diary entry for Trimester 2. Subjects who reported bleeding/spotting diary only for partial trimester are also included.
Summary of the number of days with bleeding per trimester as recorded in a daily diary. A trimester is defined as every 90 days since Day 1.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=325 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=302 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=98 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=309 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=323 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Days With Bleeding - Trimester 2 (Safety Pop.)
|
0.4 Days
Standard Deviation 2.02
|
0.2 Days
Standard Deviation 1.77
|
0.1 Days
Standard Deviation 0.42
|
0.9 Days
Standard Deviation 3.22
|
0.4 Days
Standard Deviation 1.85
|
SECONDARY outcome
Timeframe: Trimester 3Population: Subjects who had taken at least one dose (2 capsules) of IP and had at least one bleeding/spotting diary entry for Trimester 3. Subjects who reported bleeding/spotting diary only for partial trimester are also included.
Summary of the number of days with bleeding per trimester as recorded in a daily diary. A trimester is defined as every 90 days since Day 1.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=320 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=288 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=97 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=298 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=311 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Days With Bleeding - Trimester 3 (Safety Pop.)
|
0.2 Days
Standard Deviation 1.43
|
0.1 Days
Standard Deviation 0.67
|
0.0 Days
Standard Deviation 0.10
|
0.5 Days
Standard Deviation 2.32
|
0.5 Days
Standard Deviation 2.29
|
SECONDARY outcome
Timeframe: Trimester 4Population: Subjects who had taken at least one dose (2 capsules) of IP and had at least one bleeding/spotting diary entry for Trimester 4. Subjects who reported bleeding/spotting diary only for partial trimester are also included.
Summary of the number of days with bleeding per trimester as recorded in a daily diary. A trimester is defined as every 90 days since Day 1.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=308 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=276 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=282 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Number of Days With Bleeding - Trimester 4 (Safety Pop.)
|
0.2 Days
Standard Deviation 1.20
|
0.0 Days
Standard Deviation 0.26
|
0.1 Days
Standard Deviation 0.43
|
0.8 Days
Standard Deviation 3.48
|
0.4 Days
Standard Deviation 2.06
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Changes in Vasomotor Domain Score from Baseline to Week 12. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Vasomotor domain score is mean of = Q1,Q2, Q3, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=132 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=142 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=116 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=135 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Vasomotor Domain Score - Week 12 (MITT-VMS)
|
-3.3 Score on a Scale
Standard Deviation 1.97
|
-3.2 Score on a Scale
Standard Deviation 2.13
|
-2.2 Score on a Scale
Standard Deviation 1.83
|
-3.8 Score on a Scale
Standard Deviation 1.98
|
-3.3 Score on a Scale
Standard Deviation 2.04
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Changes in Vasomotor Domain Score from Baseline to Month 6. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Vasomotor domain score is mean of = Q1,Q2, Q3, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=126 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=116 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=130 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Vasomotor Domain Score - Month 6 (MITT-VMS)
|
-4.0 score on a scale
Standard Deviation 2.12
|
-3.5 score on a scale
Standard Deviation 1.95
|
-3.0 score on a scale
Standard Deviation 2.26
|
-4.3 score on a scale
Standard Deviation 1.94
|
-4.1 score on a scale
Standard Deviation 1.99
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Changes in Vasomotor Domain Score from Baseline to Month 12. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Vasomotor domain score is mean of = Q1,Q2, Q3, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=97 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Vasomotor Domain Score - Month 12 (MITT-VMS)
|
-4.0 score on a scale
Standard Deviation 2.11
|
-3.4 score on a scale
Standard Deviation 1.75
|
-2.8 score on a scale
Standard Deviation 2.26
|
-4.0 score on a scale
Standard Deviation 2.15
|
-4.1 score on a scale
Standard Deviation 1.77
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Changes in Psychosocial Domain Score from Baseline to Week 12. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Psychosocial domain score is mean of = Q4 to Q10, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=131 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=142 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=116 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=135 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Psychosocial Domain Score - Week 12 (MITT-VMS)
|
-1.2 score on a scale
Standard Deviation 1.69
|
-1.1 score on a scale
Standard Deviation 1.36
|
-1.0 score on a scale
Standard Deviation 1.66
|
-1.1 score on a scale
Standard Deviation 1.42
|
-0.9 score on a scale
Standard Deviation 1.56
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Changes in Psychosocial Domain Score from Baseline to Month 6. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Psychosocial domain score is mean of = Q4 to Q10, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=126 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=116 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=130 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Psychosocial Domain Score - Month 6 (MITT-VMS)
|
-1.1 score on a scale
Standard Deviation 1.76
|
-1.0 score on a scale
Standard Deviation 1.57
|
-1.0 score on a scale
Standard Deviation 1.61
|
-1.3 score on a scale
Standard Deviation 1.64
|
-1.1 score on a scale
Standard Deviation 1.44
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Changes in Psychosocial Domain Score from Baseline to Month 12. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Psychosocial domain score is mean of = Q4 to Q10, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=97 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Psychosocial Domain Score - Month 12 (MITT-VMS)
|
-1.1 score on a scale
Standard Deviation 1.84
|
-1.0 score on a scale
Standard Deviation 1.67
|
-1.0 score on a scale
Standard Deviation 1.61
|
-1.1 score on a scale
Standard Deviation 1.51
|
-1.3 score on a scale
Standard Deviation 1.61
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Changes in Physical Domain Score from Baseline to Week 12. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Physical domain score is mean of = Q11 to Q26, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=131 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=142 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=116 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=135 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Physical Domain Score - Week 12 (MITT-VMS)
|
-1.5 score on a scale
Standard Deviation 1.50
|
-1.0 score on a scale
Standard Deviation 1.30
|
-1.0 score on a scale
Standard Deviation 1.38
|
-1.1 score on a scale
Standard Deviation 1.30
|
-1.0 score on a scale
Standard Deviation 1.32
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Changes in Physical Domain Score from Baseline to Month 6. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Physical domain score is mean of = Q11 to Q26, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=126 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=116 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=130 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Physical Domain Score - Month 6 (MITT-VMS)
|
-1.5 score on a scale
Standard Deviation 1.61
|
-1.0 score on a scale
Standard Deviation 1.28
|
-1.1 score on a scale
Standard Deviation 1.40
|
-1.2 score on a scale
Standard Deviation 1.32
|
-1.1 score on a scale
Standard Deviation 1.37
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Changes in Physical Domain Score from Baseline to Month 12. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Physical domain score is mean of = Q11 to Q26, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=97 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Physical Domain Score - Month 12 (MITT-VMS)
|
-1.4 score on a scale
Standard Deviation 1.60
|
-1.1 score on a scale
Standard Deviation 1.44
|
-0.9 score on a scale
Standard Deviation 1.39
|
-1.0 score on a scale
Standard Deviation 1.57
|
-1.2 score on a scale
Standard Deviation 1.29
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Changes in Sexual Domain Score from Baseline to Week 12. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Sexual domain score is mean of = Q27 to Q29, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=130 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=141 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=116 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=135 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Sexual Domain Score - Week 12 (MITT-VMS)
|
-1.7 score on a scale
Standard Deviation 2.04
|
-1.4 score on a scale
Standard Deviation 2.16
|
-1.3 score on a scale
Standard Deviation 2.22
|
-1.5 score on a scale
Standard Deviation 2.03
|
-1.1 score on a scale
Standard Deviation 1.98
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Changes in Sexual Domain Score from Baseline to Month 6. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Sexual domain score is mean of = Q27 to Q29, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=125 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=115 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=130 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Sexual Domain Score - Month 6 (MITT-VMS)
|
-1.6 score on a scale
Standard Deviation 2.12
|
-1.4 score on a scale
Standard Deviation 2.13
|
-1.3 score on a scale
Standard Deviation 1.93
|
-1.3 score on a scale
Standard Deviation 2.18
|
-1.2 score on a scale
Standard Deviation 2.03
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Changes in Sexual Domain Score from Baseline to Month 12. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Sexual domain score is mean of = Q27 to Q29, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=103 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=96 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Sexual Domain Score - Month 12 (MITT-VMS)
|
-1.5 score on a scale
Standard Deviation 2.26
|
-1.4 score on a scale
Standard Deviation 2.19
|
-1.1 score on a scale
Standard Deviation 2.29
|
-1.0 score on a scale
Standard Deviation 2.44
|
-1.5 score on a scale
Standard Deviation 2.20
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Changes in Overall Scores from Baseline to Week 12. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. The scale contains four domains: vasomotor, psychosocial, physical and sexual. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The Overall Score is the mean of the 4 domain scores with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=132 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=142 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=116 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=135 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Overall Scores - Week 12 (MITT-VMS)
|
-1.9 score on a scale
Standard Deviation 1.41
|
-1.7 score on a scale
Standard Deviation 1.31
|
-1.4 score on a scale
Standard Deviation 1.36
|
-1.9 score on a scale
Standard Deviation 1.20
|
-1.6 score on a scale
Standard Deviation 1.23
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Changes in Overall Scores from Baseline to Month 6. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. The scale contains four domains: vasomotor, psychosocial, physical and sexual. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The Overall Score is the mean of the 4 domain scores with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=126 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=116 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=130 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Overall Scores - Month 6 (MITT-VMS)
|
-2.1 score on a scale
Standard Deviation 1.50
|
-1.7 score on a scale
Standard Deviation 1.24
|
-1.6 score on a scale
Standard Deviation 1.31
|
-2.0 score on a scale
Standard Deviation 1.22
|
-1.8 score on a scale
Standard Deviation 1.22
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Changes in Overall Scores from Baseline to Month 12. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. The scale contains four domains: vasomotor, psychosocial, physical and sexual. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The Overall Score is the mean of the 4 domain scores with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=97 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Overall Scores - Month 12 (MITT-VMS)
|
-2.0 score on a scale
Standard Deviation 1.50
|
-1.7 score on a scale
Standard Deviation 1.29
|
-1.5 score on a scale
Standard Deviation 1.50
|
-1.8 score on a scale
Standard Deviation 1.45
|
-2.0 score on a scale
Standard Deviation 1.27
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Wk 12 in MOS Total Sleep Score as compared w/Placebo. MOS-Sleep Self Report Questionnaire is 12 items that measure 6 dimensions of sleep over past 4 wks. Q1 scored on scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 self-reported hrs of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Total score includes items Q1, 3, 4, 5, 6, 7, 8, 9, \& 12. Scoring method: Answers to Q3, 5, 6, 7, 8, 9 are reversed \& rescaled to realign to be same direction and range (0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20. Answers to Q1, 4, \& 12 are rescaled to 0-100 as follows: MOS\_1\_new =(MOS\_1\_old - 1) x 25; MOS\_4\_new =(MOS\_4\_old - 1) x 20; MOS\_12\_new=(MOS\_12\_old - 1) x 20. Total score= average of item scores; ranges =0 to 100, where higher score means worse outcome. If any of individual questions used to obtain total score is missing, total score will be set to missing value.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=131 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=136 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=111 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=122 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=134 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Sleep Scale - Total Sleep Score - Week 12 (MITT-VMS)
|
-18.5 score on a scale
Standard Deviation 19.41
|
-14.6 score on a scale
Standard Deviation 18.80
|
-11.5 score on a scale
Standard Deviation 19.67
|
-16.7 score on a scale
Standard Deviation 16.99
|
-13.1 score on a scale
Standard Deviation 16.22
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Month 6 in MOS Total Sleep Score as compared w/Placebo. MOS-Sleep Self Report Questionnaire is 12 items that measure 6 dimensions of sleep over past 4 wks. Q1 scored on scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 self-reported hrs of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Total score includes items Q1, 3, 4, 5, 6, 7, 8, 9, \& 12. Scoring method: Answers to Q3, 5, 6, 7, 8, 9 are reversed \& rescaled to realign to be same direction and range (0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20. Answers to Q1, 4, \& 12 are rescaled to 0-100 as follows: MOS\_1\_new =(MOS\_1\_old - 1) x 25; MOS\_4\_new =(MOS\_4\_old - 1) x 20; MOS\_12\_new=(MOS\_12\_old - 1) x 20. Total score= average of item scores; ranges =0 to 100, where higher score means worse outcome. If any of individual questions used to obtain total score is missing, total score will be set to missing value.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=123 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=101 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=113 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Sleep Scale - Total Sleep Score - Month 6 (MITT-VMS)
|
-19.8 score on a scale
Standard Deviation 21.18
|
-16.6 score on a scale
Standard Deviation 19.01
|
-11.7 score on a scale
Standard Deviation 19.40
|
-17.8 score on a scale
Standard Deviation 17.28
|
-16.0 score on a scale
Standard Deviation 16.60
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Month 12 in MOS Total Sleep Score as compared w/Placebo. MOS-Sleep Self Report Questionnaire is 12 items that measure 6 dimensions of sleep over past 4 wks. Q1 scored on scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 self-reported hrs of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Total score includes items Q1, 3, 4, 5, 6, 7, 8, 9, \& 12. Scoring method: Answers to Q3, 5, 6, 7, 8, 9 are reversed \& rescaled to realign to be same direction and range (0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20. Answers to Q1, 4, \& 12 are rescaled to 0-100 as follows: MOS\_1\_new =(MOS\_1\_old - 1) x 25; MOS\_4\_new =(MOS\_4\_old - 1) x 20; MOS\_12\_new=(MOS\_12\_old - 1) x 20. Total score= average of item scores; ranges =0 to 100, where higher score means worse outcome. If any of individual questions used to obtain total score is missing, total score will be set to missing value.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=102 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=100 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=92 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=96 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=117 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Sleep Scale - Total Sleep Score - Month 12 (MITT-VMS)
|
-20.6 score on a scale
Standard Deviation 21.58
|
-17.6 score on a scale
Standard Deviation 18.81
|
-10.3 score on a scale
Standard Deviation 21.78
|
-14.9 score on a scale
Standard Deviation 21.09
|
-15.8 score on a scale
Standard Deviation 17.72
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Wk 12 in MOS Sleep Disturbance individual score as compared with Placebo. MOS-Sleep Self Report Questionnaire is 12 items that measure 6 dimensions of sleep over past 4 wks. Q1 scored on scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 self-reported hrs of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Sleep disturbance includes items Q1, Q3, Q7, Q8. Scoring method: Answer to Q1 is rescaled to 0-100 as follows: MOS\_1\_new =(MOS\_1\_old - 1) x 25. Answers to Q3, 7, 8 are reversed \& rescaled to realign to be same direction and range(0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20. Score is average of item scores; score range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=132 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=142 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=116 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=135 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Disturbance - Week 12 (MITT-VMS)
|
-23.6 score on a scale
Standard Deviation 25.07
|
-19.3 score on a scale
Standard Deviation 26.31
|
-15.1 score on a scale
Standard Deviation 26.65
|
-22.3 score on a scale
Standard Deviation 23.72
|
-17.7 score on a scale
Standard Deviation 24.75
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Month 6 in MOS Sleep Disturbance individual score as compared with Placebo. MOS-Sleep Self Report Questionnaire is 12 items that measure 6 dimensions of sleep over past 4 wks. Q1 scored on scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 self-reported hrs of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Sleep disturbance includes items Q1, Q3, Q7, Q8. Scoring method: Answer to Q1 is rescaled to 0-100 as follows: MOS\_1\_new =(MOS\_1\_old - 1) x 25. Answers to Q3, 7, 8 are reversed \& rescaled to realign to be same direction and range(0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20. Score is average of item scores; score range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=126 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=116 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=130 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Disturbance - Month 6 - (MITT-VMS)
|
-26.9 score on a scale
Standard Deviation 26.91
|
-22.4 score on a scale
Standard Deviation 26.76
|
-15.4 score on a scale
Standard Deviation 27.57
|
-23.5 score on a scale
Standard Deviation 25.99
|
-21.3 score on a scale
Standard Deviation 24.42
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Month 12 in MOS Sleep Disturbance individual score as compared with Placebo. MOS-Sleep Self Report Questionnaire is 12 items that measure 6 dimensions of sleep over past 4 wks. Q1 scored on scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 self-reported hrs of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Sleep disturbance includes items Q1, Q3, Q7, Q8. Scoring method: Answer to Q1 is rescaled to 0-100 as follows: MOS\_1\_new =(MOS\_1\_old - 1) x 25. Answers to Q3, 7, 8 are reversed \& rescaled to realign to be same direction and range(0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20. Score is average of item scores; score range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=97 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Disturbance - Month 12 - (MITT-VMS)
|
-26.1 score on a scale
Standard Deviation 27.21
|
-26.1 score on a scale
Standard Deviation 25.32
|
-14.1 score on a scale
Standard Deviation 28.67
|
-20.0 score on a scale
Standard Deviation 28.25
|
-22.3 score on a scale
Standard Deviation 24.84
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Wk 12 in MOS Snoring individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. Snoring item is Q10. Scoring method: Answer to Q10 is reversed \& rescaled to 0 to 100 such that 0="best possible" \& 100="worst possible". MOS\_n\_new \<- (6-MOS\_n\_old) x 20. Score range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=130 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=141 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=116 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=121 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=135 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Snoring - Week 12 - (MITT-VMS)
|
-7.1 score on a scale
Standard Deviation 28.49
|
-5.7 score on a scale
Standard Deviation 24.65
|
-5.7 score on a scale
Standard Deviation 25.13
|
-0.5 score on a scale
Standard Deviation 23.73
|
-3.6 score on a scale
Standard Deviation 25.84
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Month 6 in MOS Snoring individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. Snoring item is Q10. Scoring method: Answer to Q10 is reversed \& rescaled to 0 to 100 such that 0="best possible" \& 100="worst possible". MOS\_n\_new \<- (6-MOS\_n\_old) x 20. Score range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=125 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=112 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=130 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Snoring - Month 6 - (MITT-VMS)
|
-8.8 score on a scale
Standard Deviation 24.47
|
-6.1 score on a scale
Standard Deviation 30.29
|
-3.5 score on a scale
Standard Deviation 27.08
|
0.7 score on a scale
Standard Deviation 26.29
|
-5.5 score on a scale
Standard Deviation 26.24
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Month 12 in MOS Snoring individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. Snoring item is Q10. Scoring method: Answer to Q10 is reversed \& rescaled to 0 to 100 such that 0="best possible" \& 100="worst possible". MOS\_n\_new \<- (6-MOS\_n\_old) x 20. Score range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=103 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=95 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Snoring - Month 12 - (MITT-VMS)
|
-6.2 score on a scale
Standard Deviation 27.03
|
-8.0 score on a scale
Standard Deviation 26.77
|
-4.5 score on a scale
Standard Deviation 26.23
|
-1.1 score on a scale
Standard Deviation 28.04
|
-10.5 score on a scale
Standard Deviation 29.43
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Wk 12 in MOS Sleep Short of Breath or Headache(SOBHA) individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. SOBHA item is Q5. Scoring method: Answer to Q5 is reversed \& rescaled to 0 to 100 such that 0="best possible" \& 100="worst possible". MOS\_n\_new \<- (6-MOS\_n\_old) x 20. Score range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=132 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=142 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=116 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=135 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Short of Breath or Headache - Week 12 - (MITT-VMS)
|
-12.3 score on a scale
Standard Deviation 29.62
|
-7.9 score on a scale
Standard Deviation 27.67
|
-3.6 score on a scale
Standard Deviation 25.52
|
-7.7 score on a scale
Standard Deviation 26.83
|
-4.3 score on a scale
Standard Deviation 22.18
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Month 6 in MOS Sleep Short of Breath or Headache(SOBHA) individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. SOBHA item is Q5. Scoring method: Answer to Q5 is reversed \& rescaled to 0 to 100 such that 0="best possible" \& 100="worst possible". MOS\_n\_new \<- (6-MOS\_n\_old) x 20. Score range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=126 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=116 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=129 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Short of Breath or Headache - Month 6 - (MITT-VMS)
|
-11.0 score on a scale
Standard Deviation 33.55
|
-7.3 score on a scale
Standard Deviation 26.96
|
-2.1 score on a scale
Standard Deviation 23.47
|
-9.7 score on a scale
Standard Deviation 27.72
|
-5.0 score on a scale
Standard Deviation 27.50
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Month 12 in MOS Sleep Short of Breath or Headache(SOBHA) individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. SOBHA item is Q5. Scoring method: Answer to Q5 is reversed \& rescaled to 0 to 100 such that 0="best possible" \& 100="worst possible". MOS\_n\_new \<- (6-MOS\_n\_old) x 20. Score range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=103 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=97 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Short of Breath or Headache - Month 12 - (MITT-VMS)
|
-12.4 score on a scale
Standard Deviation 34.65
|
-10.8 score on a scale
Standard Deviation 27.15
|
-2.8 score on a scale
Standard Deviation 27.60
|
-8.9 score on a scale
Standard Deviation 30.41
|
-7.1 score on a scale
Standard Deviation 24.60
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Wk 12 in MOS Sleep Adequacy individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. Sleep Adequacy includes items Q4, Q12. Scoring method: Answers for Q4 and Q12 are reversed and rescaled to 0-100 as follows: MOS\_4\_new = (6-MOS\_4\_old) x 20; MOS\_12\_new = (6-MOS\_12\_old) x 20. Score is the average of item scores; score range = 0 to 100, where higher score means better outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=132 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=142 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=116 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=135 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Adequacy - Week 12 - (MITT-VMS)
|
17.3 score on a scale
Standard Deviation 30.06
|
10.7 score on a scale
Standard Deviation 28.33
|
11.3 score on a scale
Standard Deviation 26.09
|
12.8 score on a scale
Standard Deviation 28.30
|
11.0 score on a scale
Standard Deviation 26.57
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Month 6 in MOS Sleep Adequacy individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. Sleep Adequacy includes items Q4, Q12. Scoring method: Answers for Q4 and Q12 are reversed and rescaled to 0-100 as follows: MOS\_4\_new = (6-MOS\_4\_old) x 20; MOS\_12\_new = (6-MOS\_12\_old) x 20. Score is the average of item scores; score range = 0 to 100, where higher score means better outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=126 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=116 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=130 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Adequacy - Month 6 - (MITT-VMS)
|
14.7 score on a scale
Standard Deviation 30.12
|
15.2 score on a scale
Standard Deviation 28.75
|
9.5 score on a scale
Standard Deviation 27.36
|
13.2 score on a scale
Standard Deviation 28.61
|
15.2 score on a scale
Standard Deviation 26.89
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Month 12 in MOS Sleep Adequacy individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. Sleep Adequacy includes items Q4, Q12. Scoring method: Answers for Q4 and Q12 are reversed and rescaled to 0-100 as follows: MOS\_4\_new = (6-MOS\_4\_old) x 20; MOS\_12\_new = (6-MOS\_12\_old) x 20. Score is the average of item scores; score range = 0 to 100, where higher score means better outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=97 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Adequacy - Month 12 - (MITT-VMS)
|
17.6 score on a scale
Standard Deviation 31.61
|
13.7 score on a scale
Standard Deviation 27.70
|
10.0 score on a scale
Standard Deviation 31.76
|
10.4 score on a scale
Standard Deviation 28.43
|
10.5 score on a scale
Standard Deviation 31.07
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Wk 12 in MOS Sleep Somnolence individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. Sleep Somnolence items include Q6, Q9, Q11. Scoring method: Answers to Q6, Q 9 and Q11 are reversed \& rescaled to 0 to 100 such that 0="best possible" \& 100="worst possible". MOS\_n\_new \<- (6-MOS\_n\_old) x 20. Score is the average of item scores; score range range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=132 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=142 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=116 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=135 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Somnolence - Week 12 - (MITT-VMS)
|
-10.4 score on a scale
Standard Deviation 22.61
|
-10.8 score on a scale
Standard Deviation 21.78
|
-8.7 score on a scale
Standard Deviation 20.62
|
-11.3 score on a scale
Standard Deviation 20.70
|
-9.2 score on a scale
Standard Deviation 17.82
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Month 6 in MOS Sleep Somnolence individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. Sleep Somnolence items include Q6, Q9, Q11. Scoring method: Answers to Q6, Q 9 and Q11 are reversed \& rescaled to 0 to 100 such that 0="best possible" \& 100="worst possible". MOS\_n\_new \<- (6-MOS\_n\_old) x 20. Score is the average of item scores; score range range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=126 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=116 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=130 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Somnolence - Month 6 - (MITT-VMS)
|
-12.4 score on a scale
Standard Deviation 22.98
|
-10.5 score on a scale
Standard Deviation 23.69
|
-9.6 score on a scale
Standard Deviation 21.64
|
-10.1 score on a scale
Standard Deviation 21.60
|
-10.8 score on a scale
Standard Deviation 21.46
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Month 12 in MOS Sleep Somnolence individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. Sleep Somnolence items include Q6, Q9, Q11. Scoring method: Answers to Q6, Q 9 and Q11 are reversed \& rescaled to 0 to 100 such that 0="best possible" \& 100="worst possible". MOS\_n\_new \<- (6-MOS\_n\_old) x 20. Score is the average of item scores; score range range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=97 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Somnolence - Month 12 - (MITT-VMS)
|
-13.1 score on a scale
Standard Deviation 20.03
|
-13.4 score on a scale
Standard Deviation 23.82
|
-6.7 score on a scale
Standard Deviation 25.95
|
-8.0 score on a scale
Standard Deviation 22.93
|
-11.1 score on a scale
Standard Deviation 21.51
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Wk 12 in MOS Sleep Problems Index I individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Sleep Problems Index I includes items Q4, Q5, Q7, Q8, Q9, Q12. Scoring method: Answers to Q, 5, 7, 8, 9 are reversed \& rescaled to realign to be same direction and range (0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20. Answers to Q4, \& 12 are rescaled to 0-100 as follows: MOS\_4\_new =(MOS\_4\_old - 1) x 20; MOS\_12\_new=(MOS\_12\_old - 1) x 20. Score is the average of item scores; score range range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=132 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=142 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=116 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=135 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Problems Index I - Week 12 - (MITT-VMS)
|
-17.7 score on a scale
Standard Deviation 19.47
|
-13.5 score on a scale
Standard Deviation 19.65
|
-9.9 score on a scale
Standard Deviation 20.50
|
-15.2 score on a scale
Standard Deviation 17.45
|
-11.3 score on a scale
Standard Deviation 17.04
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Month 6 in MOS Sleep Problems Index I individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Sleep Problems Index I includes items Q4, Q5, Q7, Q8, Q9, Q12. Scoring method: Answers to Q, 5, 7, 8, 9 are reversed \& rescaled to realign to be same direction and range (0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20. Answers to Q4, \& 12 are rescaled to 0-100 as follows: MOS\_4\_new =(MOS\_4\_old - 1) x 20; MOS\_12\_new=(MOS\_12\_old - 1) x 20. Score is the average of item scores; score range range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=126 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=116 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=130 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Problems Index I - Month 6 - (MITT-VMS)
|
-18.0 score on a scale
Standard Deviation 20.71
|
-15.7 score on a scale
Standard Deviation 19.34
|
-9.8 score on a scale
Standard Deviation 20.37
|
-16.1 score on a scale
Standard Deviation 16.64
|
-14.3 score on a scale
Standard Deviation 16.56
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Month 12 in MOS Sleep Problems Index I individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Sleep Problems Index I includes items Q4, Q5, Q7, Q8, Q9, Q12. Scoring method: Answers to Q, 5, 7, 8, 9 are reversed \& rescaled to realign to be same direction and range (0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20. Answers to Q4, \& 12 are rescaled to 0-100 as follows: MOS\_4\_new =(MOS\_4\_old - 1) x 20; MOS\_12\_new=(MOS\_12\_old - 1) x 20. Score is the average of item scores; score range range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=97 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Problems Index I - Month 12 - (MITT-VMS)
|
-18.9 score on a scale
Standard Deviation 21.49
|
-16.1 score on a scale
Standard Deviation 20.01
|
-9.1 score on a scale
Standard Deviation 22.62
|
-13.3 score on a scale
Standard Deviation 20.52
|
-13.5 score on a scale
Standard Deviation 18.04
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Wk 12 in MOS Sleep Problems Index II individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self reported hours of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Sleep Problems Index II items include Q1, Q3, Q4, Q5, Q6, Q7, Q8, Q9, Q12. Scoring method: Answers to Q3, 5, 6, 7, 8, \& 9 are reversed \& rescaled to realign to be same direction and range 0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20, for n=Q3, 5, 6, 7, 8, and 9. Answers to Q1, 4 \& 12 are rescaled to 0-100 as follows: MOS\_1\_new =(MOS\_1\_old - 1) x 25; MOS\_4\_new =(MOS\_4\_old - 1) x 20; MOS\_12\_new=(MOS\_12\_old - 1) x 20. Score is the average of item scores; score range range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=132 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=142 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=116 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=124 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=135 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Problems Index II - Week 12 - (MITT-VMS)
|
-18.5 score on a scale
Standard Deviation 19.34
|
-14.4 score on a scale
Standard Deviation 19.19
|
-11.8 score on a scale
Standard Deviation 19.56
|
-16.8 score on a scale
Standard Deviation 17.14
|
-13.1 score on a scale
Standard Deviation 16.16
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Month 6 in MOS Sleep Problems Index II individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self reported hours of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Sleep Problems Index II items include Q1, Q3, Q4, Q5, Q6, Q7, Q8, Q9, Q12. Scoring method: Answers to Q3, 5, 6, 7, 8, \& 9 are reversed \& rescaled to realign to be same direction and range 0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20, for n=Q3, 5, 6, 7, 8, and 9. Answers to Q1, 4 \& 12 are rescaled to 0-100 as follows: MOS\_1\_new =(MOS\_1\_old - 1) x 25; MOS\_4\_new =(MOS\_4\_old - 1) x 20; MOS\_12\_new=(MOS\_12\_old - 1) x 20. Score is the average of item scores; score range range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=126 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=116 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=130 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Problems Index II - Month 6 - (MITT-VMS)
|
-19.8 score on a scale
Standard Deviation 21.18
|
-17.0 score on a scale
Standard Deviation 19.02
|
-11.6 score on a scale
Standard Deviation 19.31
|
-17.5 score on a scale
Standard Deviation 17.40
|
-16.0 score on a scale
Standard Deviation 16.69
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline to Month 12 in MOS Sleep Problems Index II individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self reported hours of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Sleep Problems Index II items include Q1, Q3, Q4, Q5, Q6, Q7, Q8, Q9, Q12. Scoring method: Answers to Q3, 5, 6, 7, 8, \& 9 are reversed \& rescaled to realign to be same direction and range 0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20, for n=Q3, 5, 6, 7, 8, and 9. Answers to Q1, 4 \& 12 are rescaled to 0-100 as follows: MOS\_1\_new =(MOS\_1\_old - 1) x 25; MOS\_4\_new =(MOS\_4\_old - 1) x 20; MOS\_12\_new=(MOS\_12\_old - 1) x 20. Score is the average of item scores; score range range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=97 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Problems Index II - Month 12 - (MITT-VMS)
|
-20.5 score on a scale
Standard Deviation 21.49
|
-17.4 score on a scale
Standard Deviation 19.48
|
-10.5 score on a scale
Standard Deviation 21.71
|
-14.7 score on a scale
Standard Deviation 21.13
|
-15.7 score on a scale
Standard Deviation 17.65
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline (BL) to Week 12 in MOS Optimal Sleep Score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items measuring 6 dimensions of sleep over the past 4 wks. Optimal sleep is based on Q2 (self-reported average hrs sleep per night in past 4 wks). Scoring method: hrs of sleep coded 0 (non-optimal) or 1 (optimal) where 1-6 hrs \& 9-23 hrs = 0, 7-8 hrs = 1. Change from BL: subject sleeps 7-8 hrs at BL \& 1-6 or 9-23 hrs at follow-up, change = -1; subject sleeps 1-6 or 9-23 hrs at BL \& 7-8 hrs at follow-up, change = +1; subject sleeps 1-6 or 9-23 hrs at BL \& 1-6 or 9-23 hrs at follow-up, change = 0. Mean change from BL: changes are summed to give the Net Total (equivalent to the number subjects w/ improved sleep hrs minus the number subjects w/ worsened sleep hrs), which is divided by the number of subjects to give the mean proportion of net change, where \>0 = overall improvement and \<0 = overall worsening in the study arm.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=132 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=142 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=115 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=123 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=134 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Optimal Sleep - Week 12 - (MITT-VMS)
|
0.2 Proportion of Net Change
Standard Deviation 0.45
|
0.2 Proportion of Net Change
Standard Deviation 0.53
|
0.2 Proportion of Net Change
Standard Deviation 0.58
|
0.2 Proportion of Net Change
Standard Deviation 0.55
|
0.2 Proportion of Net Change
Standard Deviation 0.54
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline (BL) to Month 6 in MOS Optimal Sleep Score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items measuring 6 dimensions of sleep over the past 4 wks. Optimal sleep is based on Q2 (self-reported average hrs sleep per night in past 4 wks). Scoring method: hrs of sleep coded 0 (non-optimal) or 1 (optimal) where 1-6 hrs \& 9-23 hrs = 0, 7-8 hrs = 1. Change from BL: subject sleeps 7-8 hrs at BL \& 1-6 or 9-23 hrs at follow-up, change = -1; subject sleeps 1-6 or 9-23 hrs at BL \& 7-8 hrs at follow-up, change = +1; subject sleeps 1-6 or 9-23 hrs at BL \& 1-6 or 9-23 hrs at follow-up, change = 0. Mean change from BL: changes are summed to give the Net Total (equivalent to the number subjects w/ improved sleep hrs minus the number subjects w/ worsened sleep hrs), which is divided by the number of subjects to give the mean proportion of net change, where \>0 = overall improvement and \<0 = overall worsening in the study arm.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=118 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=125 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=115 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=129 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Optimal Sleep - Month 6 - (MITT-VMS)
|
0.2 Proportion of Net Change
Standard Deviation 0.57
|
0.1 Proportion of Net Change
Standard Deviation 0.57
|
0.2 Proportion of Net Change
Standard Deviation 0.52
|
0.3 Proportion of Net Change
Standard Deviation 0.52
|
0.2 Proportion of Net Change
Standard Deviation 0.52
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: Randomized to the VMS Substudy, taken one dose of IP, and had at least 5 days of VMS diary data for baseline measurement of freq. \& severity of moderate to severe hot flushes, and had at least 4 days of VMS diary data for 1 on-treatment week of reporting freq. \& severity of hot flushes following initiation of IP.
Change from Baseline (BL) to Month 12 in MOS Optimal Sleep Score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items measuring 6 dimensions of sleep over the past 4 wks. Optimal sleep is based on Q2 (self-reported average hrs sleep per night in past 4 wks). Scoring method: hrs of sleep coded 0 (non-optimal) or 1 (optimal) where 1-6 hrs \& 9-23 hrs = 0, 7-8 hrs = 1. Change from BL: subject sleeps 7-8 hrs at BL \& 1-6 or 9-23 hrs at follow-up, change = -1; subject sleeps 1-6 or 9-23 hrs at BL \& 7-8 hrs at follow-up, change = +1; subject sleeps 1-6 or 9-23 hrs at BL \& 1-6 or 9-23 hrs at follow-up, change = 0. Mean change from BL: changes are summed to give the Net Total (equivalent to the number subjects w/ improved sleep hrs minus the number subjects w/ worsened sleep hrs), which is divided by the number of subjects to give the mean proportion of net change, where \>0 = overall improvement and \<0 = overall worsening in the study arm.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=104 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=96 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=117 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Optimal Sleep - Month 12 - (MITT-VMS)
|
0.1 Proportion of Net Change
Standard Deviation 0.57
|
0.1 Proportion of Net Change
Standard Deviation 0.51
|
0.2 Proportion of Net Change
Standard Deviation 0.47
|
0.2 Proportion of Net Change
Standard Deviation 0.47
|
0.3 Proportion of Net Change
Standard Deviation 0.58
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Changes in Vasomotor Domain Score from Baseline to Week 12. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Vasomotor domain score is mean of = Q1,Q2, Q3, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=375 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=376 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=117 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=354 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=364 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Vasomotor Domain Score - Week 12 (MITT)
|
-3.1 score on a scale
Standard Deviation 2.01
|
-2.9 score on a scale
Standard Deviation 1.94
|
-2.2 score on a scale
Standard Deviation 1.84
|
-3.5 score on a scale
Standard Deviation 2.02
|
-3.1 score on a scale
Standard Deviation 2.00
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Changes in Vasomotor Domain Score from Baseline to Month 6. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Vasomotor domain score is mean of = Q1,Q2, Q3, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=342 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=324 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=316 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=333 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Vasomotor Domain Score - Month 6 (MITT)
|
-3.5 score on a scale
Standard Deviation 2.15
|
-3.3 score on a scale
Standard Deviation 1.94
|
-3.0 score on a scale
Standard Deviation 2.26
|
-4.0 score on a scale
Standard Deviation 1.95
|
-3.7 score on a scale
Standard Deviation 2.02
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Changes in Vasomotor Domain Score from Baseline to Month 12. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Vasomotor domain score is mean of = Q1,Q2, Q3, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=312 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=280 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=283 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Vasomotor Domain Score - Month 12 (MITT)
|
-3.4 score on a scale
Standard Deviation 2.06
|
-3.3 score on a scale
Standard Deviation 1.80
|
-2.8 score on a scale
Standard Deviation 2.26
|
-3.8 score on a scale
Standard Deviation 2.05
|
-3.7 score on a scale
Standard Deviation 1.89
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Changes in Psychosocial Domain Score from Baseline to Week 12. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Psychosocial domain score is mean of = Q4 to Q10, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=373 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=376 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=117 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=354 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=363 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Psychosocial Domain Score - Week 12 (MITT)
|
-1.1 score on a scale
Standard Deviation 1.58
|
-1.0 score on a scale
Standard Deviation 1.49
|
-1.0 score on a scale
Standard Deviation 1.68
|
-1.1 score on a scale
Standard Deviation 1.52
|
-1.0 score on a scale
Standard Deviation 1.66
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Changes in Psychosocial Domain Score from Baseline to Month 6. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Psychosocial domain score is mean of = Q4 to Q10, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=343 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=324 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=316 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=330 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Psychosocial Domain Score - Month 6 (MITT)
|
-1.1 score on a scale
Standard Deviation 1.65
|
-1.0 score on a scale
Standard Deviation 1.55
|
-1.0 score on a scale
Standard Deviation 1.61
|
-1.3 score on a scale
Standard Deviation 1.68
|
-1.1 score on a scale
Standard Deviation 1.65
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Changes in Psychosocial Domain Score from Baseline to Month 12. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Psychosocial domain score is mean of = Q4 to Q10, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=312 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=280 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=282 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=303 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Psychosocial Domain Score - Month 12 (MITT)
|
-1.1 score on a scale
Standard Deviation 1.66
|
-1.0 score on a scale
Standard Deviation 1.64
|
-1.0 score on a scale
Standard Deviation 1.61
|
-1.1 score on a scale
Standard Deviation 1.65
|
-1.1 score on a scale
Standard Deviation 1.74
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Changes in Physical Domain Score from Baseline to Week 12. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Physical domain score is mean of = Q11 to Q26, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=374 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=376 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=117 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=354 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=364 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Physical Domain Score - Week 12 (MITT)
|
-1.3 score on a scale
Standard Deviation 1.40
|
-1.1 score on a scale
Standard Deviation 1.39
|
-1.0 score on a scale
Standard Deviation 1.38
|
-1.1 score on a scale
Standard Deviation 1.41
|
-1.1 score on a scale
Standard Deviation 1.44
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Changes in Physical Domain Score from Baseline to Month 6. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Physical domain score is mean of = Q11 to Q26, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=343 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=324 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=316 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=332 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Physical Domain Score - Month 6 (MITT)
|
-1.2 score on a scale
Standard Deviation 1.46
|
-1.0 score on a scale
Standard Deviation 1.39
|
-1.1 score on a scale
Standard Deviation 1.40
|
-1.2 score on a scale
Standard Deviation 1.42
|
-1.1 score on a scale
Standard Deviation 1.46
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Changes in Physical Domain Score from Baseline to Month 12. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Physical domain score is mean of = Q11 to Q26, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=312 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=280 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=282 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Physical Domain Score - Month 12 (MITT)
|
-1.2 score on a scale
Standard Deviation 1.43
|
-1.1 score on a scale
Standard Deviation 1.50
|
-0.9 score on a scale
Standard Deviation 1.39
|
-1.1 score on a scale
Standard Deviation 1.52
|
-1.1 score on a scale
Standard Deviation 1.48
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Changes in Sexual Domain Score from Baseline to Week 12. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Sexual domain score is mean of = Q27 to Q29, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=371 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=375 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=117 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=352 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=364 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Sexual Domain Score - Week 12 (MITT)
|
-1.5 score on a scale
Standard Deviation 2.02
|
-1.5 score on a scale
Standard Deviation 2.15
|
-1.3 score on a scale
Standard Deviation 2.21
|
-1.4 score on a scale
Standard Deviation 2.06
|
-1.3 score on a scale
Standard Deviation 2.21
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Changes in Sexual Domain Score from Baseline to Month 6. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Sexual domain score is mean of = Q27 to Q29, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=342 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=322 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=315 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=332 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Sexual Domain Score - Month 6 (MITT)
|
-1.4 score on a scale
Standard Deviation 2.05
|
-1.3 score on a scale
Standard Deviation 2.10
|
-1.3 score on a scale
Standard Deviation 1.93
|
-1.4 score on a scale
Standard Deviation 2.11
|
-1.4 score on a scale
Standard Deviation 2.12
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Changes in Sexual Domain Score from Baseline to Month 12. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The scale contains four domains: vasomotor, psychosocial, physical and sexual. Each domain is scored separately. Sexual domain score is mean of = Q27 to Q29, with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=310 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=278 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=281 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Sexual Domain Score - Month 12 (MITT)
|
-1.3 score on a scale
Standard Deviation 2.10
|
-1.2 score on a scale
Standard Deviation 2.25
|
-1.1 score on a scale
Standard Deviation 2.29
|
-1.3 score on a scale
Standard Deviation 2.26
|
-1.4 score on a scale
Standard Deviation 2.32
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change in Overall Scores from Baseline to Week 12. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. The scale contains four domains: vasomotor, psychosocial, physical and sexual. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The Overall Score is the mean of the 4 domain scores with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=375 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=376 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=117 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=354 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=364 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Overall Scores - Week 12 (MITT)
|
-1.7 score on a scale
Standard Deviation 1.35
|
-1.6 score on a scale
Standard Deviation 1.35
|
-1.4 score on a scale
Standard Deviation 1.36
|
-1.8 score on a scale
Standard Deviation 1.31
|
-1.6 score on a scale
Standard Deviation 1.38
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change in Overall Scores from Baseline to Month 6. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. The scale contains four domains: vasomotor, psychosocial, physical and sexual. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The Overall Score is the mean of the 4 domain scores with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=343 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=324 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=316 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=333 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Overall Scores - Month 6 (MITT)
|
-1.8 score on a scale
Standard Deviation 1.39
|
-1.7 score on a scale
Standard Deviation 1.29
|
-1.6 score on a scale
Standard Deviation 1.31
|
-2.0 score on a scale
Standard Deviation 1.32
|
-1.8 score on a scale
Standard Deviation 1.38
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change in Overall Scores from Baseline to Month 12. The MENQOL is self-administered questionnaire which assessed changes in quality of life over a one-month period. It is composed of 29 questions indicating if subject experienced the problem (Yes/No) and if Yes, rating scale ranged from 0=Not bothered at all to 6=Extremely bothered. The scale contains four domains: vasomotor, psychosocial, physical and sexual. For analysis, the original scores were converted to the analysis score ranging from 1-8 where No=1, 0=2, 1=3...and 6=8. The Overall Score is the mean of the 4 domain scores with 1 being "not at all bothered" and 8 being "extremely bothered".
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=312 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=280 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=283 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=304 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Menopause-specific Quality of Life Questionnaire (MENQOL) - Overall Scores - Month 12 (MITT)
|
-1.7 score on a scale
Standard Deviation 1.38
|
-1.6 score on a scale
Standard Deviation 1.38
|
-1.5 score on a scale
Standard Deviation 1.50
|
-1.8 score on a scale
Standard Deviation 1.43
|
-1.8 score on a scale
Standard Deviation 1.45
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Wk 12 in MOS Total Sleep Score as compared w/Placebo. MOS-Sleep Self Report Questionnaire is 12 items that measure 6 dimensions of sleep over past 4 wks. Q1 scored on scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 self-reported hrs of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Total score includes items Q1, 3, 4, 5, 6, 7, 8, 9, \& 12. Scoring method: Answers to Q3, 5, 6, 7, 8, 9 are reversed \& rescaled to realign to be same direction and range (0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20. Answers to Q1, 4, \& 12 are rescaled to 0-100 as follows: MOS\_1\_new =(MOS\_1\_old - 1) x 25; MOS\_4\_new =(MOS\_4\_old - 1) x 20; MOS\_12\_new=(MOS\_12\_old - 1) x 20. Total score= average of item scores; ranges =0 to 100, where higher score means worse outcome. If any of individual questions used to obtain total score is missing, total score will be set to missing value.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=370 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=365 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=112 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=350 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=358 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Sleep Scale - Total Sleep Score - Week 12 (MITT)
|
-13.9 score on a scale
Standard Deviation 17.40
|
-13.3 score on a scale
Standard Deviation 18.22
|
-11.5 score on a scale
Standard Deviation 19.60
|
-15.1 score on a scale
Standard Deviation 17.64
|
-13.0 score on a scale
Standard Deviation 17.42
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Month 6 in MOS Total Sleep Score as compared w/Placebo. MOS-Sleep Self Report Questionnaire is 12 items that measure 6 dimensions of sleep over past 4 wks. Q1 scored on scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 self-reported hrs of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Total score includes items Q1, 3, 4, 5, 6, 7, 8, 9, \& 12. Scoring method: Answers to Q3, 5, 6, 7, 8, 9 are reversed \& rescaled to realign to be same direction and range (0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20. Answers to Q1, 4, \& 12 are rescaled to 0-100 as follows: MOS\_1\_new =(MOS\_1\_old - 1) x 25; MOS\_4\_new =(MOS\_4\_old - 1) x 20; MOS\_12\_new=(MOS\_12\_old - 1) x 20. Total score= average of item scores; ranges =0 to 100, where higher score means worse outcome. If any of individual questions used to obtain total score is missing, total score will be set to missing value.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=339 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=317 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=101 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=313 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=321 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Sleep Scale - Total Sleep Score - Month 6 (MITT)
|
-14.7 score on a scale
Standard Deviation 18.95
|
-14.6 score on a scale
Standard Deviation 18.93
|
-11.7 score on a scale
Standard Deviation 19.40
|
-15.6 score on a scale
Standard Deviation 18.13
|
-14.8 score on a scale
Standard Deviation 16.10
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Month 12 in MOS Total Sleep Score as compared w/Placebo. MOS-Sleep Self Report Questionnaire is 12 items that measure 6 dimensions of sleep over past 4 wks. Q1 scored on scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 self-reported hrs of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Total score includes items Q1, 3, 4, 5, 6, 7, 8, 9, \& 12. Scoring method: Answers to Q3, 5, 6, 7, 8, 9 are reversed \& rescaled to realign to be same direction and range (0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20. Answers to Q1, 4, \& 12 are rescaled to 0-100 as follows: MOS\_1\_new =(MOS\_1\_old - 1) x 25; MOS\_4\_new =(MOS\_4\_old - 1) x 20; MOS\_12\_new=(MOS\_12\_old - 1) x 20. Total score= average of item scores; ranges =0 to 100, where higher score means worse outcome. If any of individual questions used to obtain total score is missing, total score will be set to missing value.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=308 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=270 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=92 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=281 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=300 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Sleep Scale - Total Sleep Score - Month 12 (MITT)
|
-15.3 score on a scale
Standard Deviation 18.78
|
-15.3 score on a scale
Standard Deviation 19.28
|
-10.3 score on a scale
Standard Deviation 21.78
|
-14.4 score on a scale
Standard Deviation 18.36
|
-14.5 score on a scale
Standard Deviation 17.85
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Wk 12 in MOS Sleep Disturbance individual score as compared with Placebo. MOS-Sleep Self Report Questionnaire is 12 items that measure 6 dimensions of sleep over past 4 wks. Q1 scored on scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 self-reported hrs of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Sleep disturbance includes items Q1, Q3, Q7, Q8. Scoring method: Answer to Q1 is rescaled to 0-100 as follows: MOS\_1\_new =(MOS\_1\_old - 1) x 25. Answers to Q3, 7, 8 are reversed \& rescaled to realign to be same direction and range(0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20. Score is average of item scores; score range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=374 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=376 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=117 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=354 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=365 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Disturbance - Week 12 - (MITT)
|
-18.7 score on a scale
Standard Deviation 23.11
|
-17.3 score on a scale
Standard Deviation 24.88
|
-14.9 score on a scale
Standard Deviation 26.57
|
-21.0 score on a scale
Standard Deviation 23.74
|
-18.1 score on a scale
Standard Deviation 24.62
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Month 6 in MOS Sleep Disturbance individual score as compared with Placebo. MOS-Sleep Self Report Questionnaire is 12 items that measure 6 dimensions of sleep over past 4 wks. Q1 scored on scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 self-reported hrs of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Sleep disturbance includes items Q1, Q3, Q7, Q8. Scoring method: Answer to Q1 is rescaled to 0-100 as follows: MOS\_1\_new =(MOS\_1\_old - 1) x 25. Answers to Q3, 7, 8 are reversed \& rescaled to realign to be same direction and range(0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20. Score is average of item scores; score range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=343 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=324 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=317 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=333 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Disturbance - Month 6 - (MITT)
|
-20.1 score on a scale
Standard Deviation 25.12
|
-19.4 score on a scale
Standard Deviation 24.85
|
-15.4 score on a scale
Standard Deviation 27.57
|
-22.3 score on a scale
Standard Deviation 25.24
|
-20.2 score on a scale
Standard Deviation 22.46
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Month 12 in MOS Sleep Disturbance individual score as compared with Placebo. MOS-Sleep Self Report Questionnaire is 12 items that measure 6 dimensions of sleep over past 4 wks. Q1 scored on scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 self-reported hrs of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Sleep disturbance includes items Q1, Q3, Q7, Q8. Scoring method: Answer to Q1 is rescaled to 0-100 as follows: MOS\_1\_new =(MOS\_1\_old - 1) x 25. Answers to Q3, 7, 8 are reversed \& rescaled to realign to be same direction and range(0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20. Score is average of item scores; score range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=312 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=280 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=283 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=305 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Disturbance - Month 12 - (MITT)
|
-19.9 score on a scale
Standard Deviation 25.01
|
-19.7 score on a scale
Standard Deviation 24.13
|
-14.1 score on a scale
Standard Deviation 28.67
|
-20.2 score on a scale
Standard Deviation 25.27
|
-19.9 score on a scale
Standard Deviation 24.90
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Wk 12 in MOS Snoring individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. Snoring item is Q10. Scoring method: Answer to Q10 is reversed \& rescaled to 0 to 100 such that 0="best possible" \& 100="worst possible". MOS\_n\_new \<- (6-MOS\_n\_old) x 20. Score range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=371 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=375 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=117 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=351 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=364 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Snoring - Week 12 - (MITT)
|
-4.5 score on a scale
Standard Deviation 28.93
|
-3.4 score on a scale
Standard Deviation 26.94
|
-5.6 score on a scale
Standard Deviation 25.03
|
-2.6 score on a scale
Standard Deviation 25.30
|
-4.7 score on a scale
Standard Deviation 26.08
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Month 6 in MOS Snoring individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. Snoring item is Q10. Scoring method: Answer to Q10 is reversed \& rescaled to 0 to 100 such that 0="best possible" \& 100="worst possible". MOS\_n\_new \<- (6-MOS\_n\_old) x 20. Score range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=340 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=323 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=312 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=332 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Snoring - Month 6 - (MITT)
|
-6.8 score on a scale
Standard Deviation 27.32
|
-3.7 score on a scale
Standard Deviation 28.98
|
-3.5 score on a scale
Standard Deviation 27.08
|
-2.4 score on a scale
Standard Deviation 28.00
|
-6.0 score on a scale
Standard Deviation 25.73
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Month 12 in MOS Snoring individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. Snoring item is Q10. Scoring method: Answer to Q10 is reversed \& rescaled to 0 to 100 such that 0="best possible" \& 100="worst possible". MOS\_n\_new \<- (6-MOS\_n\_old) x 20. Score range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=311 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=277 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=280 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=305 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Snoring - Month 12 - (MITT)
|
-5.0 score on a scale
Standard Deviation 28.57
|
-4.5 score on a scale
Standard Deviation 24.79
|
-4.5 score on a scale
Standard Deviation 26.23
|
-3.4 score on a scale
Standard Deviation 29.62
|
-7.5 score on a scale
Standard Deviation 27.71
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Wk 12 in MOS Sleep Short of Breath or Headache(SOBHA) individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. SOBHA item is Q5. Scoring method: Answer to Q5 is reversed \& rescaled to 0 to 100 such that 0="best possible" \& 100="worst possible". MOS\_n\_new \<- (6-MOS\_n\_old) x 20. Score range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=374 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=376 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=117 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=354 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=364 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Short of Breath or Headache - Week 12 - (MITT)
|
-7.1 score on a scale
Standard Deviation 27.97
|
-6.3 score on a scale
Standard Deviation 27.03
|
-3.4 score on a scale
Standard Deviation 25.50
|
-6.0 score on a scale
Standard Deviation 24.56
|
-6.0 score on a scale
Standard Deviation 23.67
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Month 6 in MOS Sleep Short of Breath or Headache(SOBHA) individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. SOBHA item is Q5. Scoring method: Answer to Q5 is reversed \& rescaled to 0 to 100 such that 0="best possible" \& 100="worst possible". MOS\_n\_new \<- (6-MOS\_n\_old) x 20. Score range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=343 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=324 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=317 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=332 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Short of Breath or Headache - Month 6 - (MITT)
|
-7.5 score on a scale
Standard Deviation 27.19
|
-5.7 score on a scale
Standard Deviation 26.34
|
-2.1 score on a scale
Standard Deviation 23.47
|
-6.2 score on a scale
Standard Deviation 28.14
|
-5.9 score on a scale
Standard Deviation 24.36
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Month 12 in MOS Sleep Short of Breath or Headache(SOBHA) individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. SOBHA item is Q5. Scoring method: Answer to Q5 is reversed \& rescaled to 0 to 100 such that 0="best possible" \& 100="worst possible". MOS\_n\_new \<- (6-MOS\_n\_old) x 20. Score range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=311 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=280 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=283 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=305 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Short of Breath or Headache - Month 12 - (MITT)
|
-7.9 score on a scale
Standard Deviation 28.34
|
-6.5 score on a scale
Standard Deviation 28.07
|
-2.8 score on a scale
Standard Deviation 27.60
|
-6.6 score on a scale
Standard Deviation 27.64
|
-6.4 score on a scale
Standard Deviation 23.58
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Wk 12 in MOS Sleep Adequacy individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. Sleep Adequacy includes items Q4, Q12. Scoring method: Answers for Q4 and Q12 are reversed and rescaled to 0-100 as follows: MOS\_4\_new = (6-MOS\_4\_old) x 20; MOS\_12\_new = (6-MOS\_12\_old) x 20. Score is the average of item scores; score range = 0 to 100, where higher score means better outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=374 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=376 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=117 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=354 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=365 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Adequacy - Week 12 - (MITT)
|
11.4 score on a scale
Standard Deviation 27.54
|
11.9 score on a scale
Standard Deviation 27.30
|
11.3 score on a scale
Standard Deviation 25.98
|
11.9 score on a scale
Standard Deviation 29.12
|
9.0 score on a scale
Standard Deviation 27.40
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Month 6 in MOS Sleep Adequacy individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. Sleep Adequacy includes items Q4, Q12. Scoring method: Answers for Q4 and Q12 are reversed and rescaled to 0-100 as follows: MOS\_4\_new = (6-MOS\_4\_old) x 20; MOS\_12\_new = (6-MOS\_12\_old) x 20. Score is the average of item scores; score range = 0 to 100, where higher score means better outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=343 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=324 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=317 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=333 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Adequacy - Month 6 - (MITT)
|
11.0 score on a scale
Standard Deviation 28.85
|
14.5 score on a scale
Standard Deviation 27.92
|
9.5 score on a scale
Standard Deviation 27.36
|
10.5 score on a scale
Standard Deviation 26.86
|
11.7 score on a scale
Standard Deviation 28.11
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Month 12 in MOS Sleep Adequacy individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. Sleep Adequacy includes items Q4, Q12. Scoring method: Answers for Q4 and Q12 are reversed and rescaled to 0-100 as follows: MOS\_4\_new = (6-MOS\_4\_old) x 20; MOS\_12\_new = (6-MOS\_12\_old) x 20. Score is the average of item scores; score range = 0 to 100, where higher score means better outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=312 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=280 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=283 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=305 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Adequacy - Month 12 - (MITT)
|
12.6 score on a scale
Standard Deviation 27.71
|
14.1 score on a scale
Standard Deviation 28.81
|
10.0 score on a scale
Standard Deviation 31.76
|
9.8 score on a scale
Standard Deviation 27.33
|
12.0 score on a scale
Standard Deviation 29.86
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Wk 12 in MOS Sleep Somnolence individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. Sleep Somnolence items include Q6, Q9, Q11. Scoring method: Answers to Q6, Q 9 and Q11 are reversed \& rescaled to 0 to 100 such that 0="best possible" \& 100="worst possible". MOS\_n\_new \<- (6-MOS\_n\_old) x 20. Score is the average of item scores; score range range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=374 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=376 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=117 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=354 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=365 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Somnolence - Week 12 - (MITT)
|
-7.6 score on a scale
Standard Deviation 19.57
|
-8.9 score on a scale
Standard Deviation 21.09
|
-8.7 score on a scale
Standard Deviation 20.54
|
-9.2 score on a scale
Standard Deviation 20.49
|
-8.1 score on a scale
Standard Deviation 18.67
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Month 6 in MOS Sleep Somnolence individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. Sleep Somnolence items include Q6, Q9, Q11. Scoring method: Answers to Q6, Q 9 and Q11 are reversed \& rescaled to 0 to 100 such that 0="best possible" \& 100="worst possible". MOS\_n\_new \<- (6-MOS\_n\_old) x 20. Score is the average of item scores; score range range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=343 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=324 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=317 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=333 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Somnolence - Month 6 - (MITT)
|
-9.6 score on a scale
Standard Deviation 20.04
|
-8.7 score on a scale
Standard Deviation 21.65
|
-9.6 score on a scale
Standard Deviation 21.64
|
-9.4 score on a scale
Standard Deviation 22.40
|
-8.4 score on a scale
Standard Deviation 19.88
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Month 12 in MOS Sleep Somnolence individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-Q12 are scored 1-6 ranging from 1=All of the time to 6=None of the time. Sleep Somnolence items include Q6, Q9, Q11. Scoring method: Answers to Q6, Q 9 and Q11 are reversed \& rescaled to 0 to 100 such that 0="best possible" \& 100="worst possible". MOS\_n\_new \<- (6-MOS\_n\_old) x 20. Score is the average of item scores; score range range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=312 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=280 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=283 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=305 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Somnolence - Month 12 - (MITT)
|
-9.9 score on a scale
Standard Deviation 19.33
|
-9.4 score on a scale
Standard Deviation 23.06
|
-6.7 score on a scale
Standard Deviation 25.95
|
-8.5 score on a scale
Standard Deviation 22.79
|
-9.2 score on a scale
Standard Deviation 19.17
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Wk 12 in MOS Sleep Problems Index I individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Sleep Problems Index I includes items Q4, Q5, Q7, Q8, Q9, Q12. Scoring method: Answers to Q, 5, 7, 8, 9 are reversed \& rescaled to realign to be same direction and range (0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20. Answers to Q4, \& 12 are rescaled to 0-100 as follows: MOS\_4\_new =(MOS\_4\_old - 1) x 20; MOS\_12\_new=(MOS\_12\_old - 1) x 20. Score is the average of item scores; score range range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=374 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=376 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=117 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=354 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=365 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Problems Index I - Week 12 - (MITT)
|
-12.2 score on a scale
Standard Deviation 18.29
|
-12.8 score on a scale
Standard Deviation 19.33
|
-9.8 score on a scale
Standard Deviation 20.47
|
-13.5 score on a scale
Standard Deviation 17.90
|
-11.4 score on a scale
Standard Deviation 18.02
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Month 6 in MOS Sleep Problems Index I individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Sleep Problems Index I includes items Q4, Q5, Q7, Q8, Q9, Q12. Scoring method: Answers to Q, 5, 7, 8, 9 are reversed \& rescaled to realign to be same direction and range (0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20. Answers to Q4, \& 12 are rescaled to 0-100 as follows: MOS\_4\_new =(MOS\_4\_old - 1) x 20; MOS\_12\_new=(MOS\_12\_old - 1) x 20. Score is the average of item scores; score range range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=343 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=324 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=317 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=333 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Problems Index I - Month 6 - (MITT)
|
-13.2 score on a scale
Standard Deviation 19.16
|
-13.8 score on a scale
Standard Deviation 19.77
|
-9.8 score on a scale
Standard Deviation 20.37
|
-14.0 score on a scale
Standard Deviation 17.60
|
-12.9 score on a scale
Standard Deviation 16.76
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Month 12 in MOS Sleep Problems Index I individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self-reported hours of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Sleep Problems Index I includes items Q4, Q5, Q7, Q8, Q9, Q12. Scoring method: Answers to Q, 5, 7, 8, 9 are reversed \& rescaled to realign to be same direction and range (0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20. Answers to Q4, \& 12 are rescaled to 0-100 as follows: MOS\_4\_new =(MOS\_4\_old - 1) x 20; MOS\_12\_new=(MOS\_12\_old - 1) x 20. Score is the average of item scores; score range range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=312 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=280 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=283 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=305 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Problems Index I - Month 12 - (MITT)
|
-13.7 score on a scale
Standard Deviation 19.02
|
-14.0 score on a scale
Standard Deviation 20.14
|
-9.1 score on a scale
Standard Deviation 22.62
|
-12.8 score on a scale
Standard Deviation 18.19
|
-13.0 score on a scale
Standard Deviation 18.36
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Wk 12 in MOS Sleep Problems Index II individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self reported hours of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Sleep Problems Index II items include Q1, Q3, Q4, Q5, Q6, Q7, Q8, Q9, Q12. Scoring method: Answers to Q3, 5, 6, 7, 8, \& 9 are reversed \& rescaled to realign to be same direction and range 0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20, for n=Q3, 5, 6, 7, 8, and 9. Answers to Q1, 4 \& 12 are rescaled to 0-100 as follows: MOS\_1\_new =(MOS\_1\_old - 1) x 25; MOS\_4\_new =(MOS\_4\_old - 1) x 20; MOS\_12\_new=(MOS\_12\_old - 1) x 20. Score is the average of item scores; score range range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=374 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=376 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=117 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=354 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=365 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Problems Index II - Week 12 - (MITT)
|
-13.9 score on a scale
Standard Deviation 17.40
|
-13.4 score on a scale
Standard Deviation 18.47
|
-11.8 score on a scale
Standard Deviation 19.48
|
-15.1 score on a scale
Standard Deviation 17.64
|
-13.0 score on a scale
Standard Deviation 17.38
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Month 6 in MOS Sleep Problems Index II individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self reported hours of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Sleep Problems Index II items include Q1, Q3, Q4, Q5, Q6, Q7, Q8, Q9, Q12. Scoring method: Answers to Q3, 5, 6, 7, 8, \& 9 are reversed \& rescaled to realign to be same direction and range 0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20, for n=Q3, 5, 6, 7, 8, and 9. Answers to Q1, 4 \& 12 are rescaled to 0-100 as follows: MOS\_1\_new =(MOS\_1\_old - 1) x 25; MOS\_4\_new =(MOS\_4\_old - 1) x 20; MOS\_12\_new=(MOS\_12\_old - 1) x 20. Score is the average of item scores; score range range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=343 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=324 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=317 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=333 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Sleep Problems Index II - Month 6 - (MITT)
|
-14.9 score on a scale
Standard Deviation 18.95
|
-14.8 score on a scale
Standard Deviation 18.87
|
-11.6 score on a scale
Standard Deviation 19.31
|
-15.5 score on a scale
Standard Deviation 18.15
|
-14.6 score on a scale
Standard Deviation 16.41
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline to Month 12 in MOS Sleep Problems Index II individual score as compared with Placebo. The MOS-Sleep Self Report Questionnaire is composed of 12 items that measure 6 dimensions of sleep over the past 4 weeks. Q1 is scored on a scale 1-5: 1=0-15 min, 2=16-30 min...5=\>60 mins. Q2 is self reported hours of sleep per night. Q3-12 scored 1-6 where 1=All of the time to 6=None of the time. Sleep Problems Index II items include Q1, Q3, Q4, Q5, Q6, Q7, Q8, Q9, Q12. Scoring method: Answers to Q3, 5, 6, 7, 8, \& 9 are reversed \& rescaled to realign to be same direction and range 0 to 100 with 0="best possible" \& 100="worst possible" as follows: MOS\_n\_new = (6-MOS\_n\_old) x 20, for n=Q3, 5, 6, 7, 8, and 9. Answers to Q1, 4 \& 12 are rescaled to 0-100 as follows: MOS\_1\_new =(MOS\_1\_old - 1) x 25; MOS\_4\_new =(MOS\_4\_old - 1) x 20; MOS\_12\_new=(MOS\_12\_old - 1) x 20. Score is the average of item scores; score range range=0 to 100, where higher score means worse outcome.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=312 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=280 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=283 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=305 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Individual Score for Sleep Problems Index II - Month 12 - (MITT)
|
-15.4 score on a scale
Standard Deviation 18.74
|
-15.1 score on a scale
Standard Deviation 19.43
|
-10.5 score on a scale
Standard Deviation 21.71
|
-14.3 score on a scale
Standard Deviation 18.35
|
-14.6 score on a scale
Standard Deviation 17.95
|
SECONDARY outcome
Timeframe: Baseline and Week 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline (BL) to Wk 12 in MOS Optimal Sleep Score as compared with Placebo.The MOS-Sleep Self Report Questionnaire is composed of 12 items measuring 6 dimensions of sleep over the past 4 wks. Optimal sleep is based on Q2 (self-reported average hrs sleep per night in past 4 wks). Scoring method: hrs of sleep coded 0 (non-optimal) or 1 (optimal) where 1-6 hrs \& 9-23 hrs = 0, 7-8 hrs = 1. Change from BL: subject sleeps 7-8 hrs at BL \& 1-6 or 9-23 hrs at follow-up, change = -1; subject sleeps 1-6 or 9-23 hrs at BL \& 7-8 hrs at follow-up, change = +1; subject sleeps 1-6 or 9-23 hrs at BL \& 1-6 or 9-23 hrs at follow-up, change = 0. Mean change from BL: changes are summed to give the Net Total (equivalent to the number subjects w/ improved sleep hrs minus the number subjects w/ worsened sleep hrs), which is divided by the number of subjects to give the mean proportion of net change, where \>0 = overall improvement and \<0 = overall worsening in the study arm.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=372 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=376 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=116 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=353 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=364 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Optimal Sleep - Week 12 - (MITT)
|
0.2 Proportion of Net Change
Standard Deviation 0.49
|
0.1 Proportion of Net Change
Standard Deviation 0.52
|
0.2 Proportion of Net Change
Standard Deviation 0.59
|
0.2 Proportion of Net Change
Standard Deviation 0.53
|
0.1 Proportion of Net Change
Standard Deviation 0.56
|
SECONDARY outcome
Timeframe: Baseline and Month 6Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline (BL) to Month 6 in MOS Optimal Sleep Score as compared with Placebo.The MOS-Sleep Self Report Questionnaire is composed of 12 items measuring 6 dimensions of sleep over the past 4 wks. Optimal sleep is based on Q2 (self-reported average hrs sleep per night in past 4 wks). Scoring method: hrs of sleep coded 0 (non-optimal) or 1 (optimal) where 1-6 hrs \& 9-23 hrs = 0, 7-8 hrs = 1. Change from BL: subject sleeps 7-8 hrs at BL \& 1-6 or 9-23 hrs at follow-up, change = -1; subject sleeps 1-6 or 9-23 hrs at BL \& 7-8 hrs at follow-up, change = +1; subject sleeps 1-6 or 9-23 hrs at BL \& 1-6 or 9-23 hrs at follow-up, change = 0. Mean change from BL: changes are summed to give the Net Total (equivalent to the number subjects w/ improved sleep hrs minus the number subjects w/ worsened sleep hrs), which is divided by the number of subjects to give the mean proportion of net change, where \>0 = overall improvement and \<0 = overall worsening in the study arm.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=339 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=323 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=104 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=316 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=331 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Optimal Sleep - Month 6 - (MITT)
|
0.2 Proportion of Net Change
Standard Deviation 0.53
|
0.1 Proportion of Net Change
Standard Deviation 0.56
|
0.2 Proportion of Net Change
Standard Deviation 0.52
|
0.2 Proportion of Net Change
Standard Deviation 0.56
|
0.2 Proportion of Net Change
Standard Deviation 0.55
|
SECONDARY outcome
Timeframe: Baseline and Month 12Population: All randomized subjects who took at least one dose (2 capsules) of IP.
Change from Baseline (BL) to Month 12 in MOS Optimal Sleep Score as compared with Placebo.The MOS-Sleep Self Report Questionnaire is composed of 12 items measuring 6 dimensions of sleep over the past 4 wks. Optimal sleep is based on Q2 (self-reported average hrs sleep per night in past 4 wks). Scoring method: hrs of sleep coded 0 (non-optimal) or 1 (optimal) where 1-6 hrs \& 9-23 hrs = 0, 7-8 hrs = 1. Change from BL: subject sleeps 7-8 hrs at BL \& 1-6 or 9-23 hrs at follow-up, change = -1; subject sleeps 1-6 or 9-23 hrs at BL \& 7-8 hrs at follow-up, change = +1; subject sleeps 1-6 or 9-23 hrs at BL \& 1-6 or 9-23 hrs at follow-up, change = 0. Mean change from BL: changes are summed to give the Net Total (equivalent to the number subjects w/ improved sleep hrs minus the number subjects w/ worsened sleep hrs), which is divided by the number of subjects to give the mean proportion of net change, where \>0 = overall improvement and \<0 = overall worsening in the study arm.
Outcome measures
| Measure |
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=311 Participants
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=280 Participants
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=93 Participants
Two Placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 1 mg / Progesterone 100 mg
n=282 Participants
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=303 Participants
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Medical Outcomes Sleep Study (MOS) Optimal Sleep - Month 12 - (MITT)
|
0.1 Proportion of Net Change
Standard Deviation 0.55
|
0.1 Proportion of Net Change
Standard Deviation 0.52
|
0.2 Proportion of Net Change
Standard Deviation 0.47
|
0.1 Proportion of Net Change
Standard Deviation 0.51
|
0.2 Proportion of Net Change
Standard Deviation 0.56
|
Adverse Events
Combined Estradiol 1 mg / Progesterone 100 mg
Combined Estradiol 0.5 mg / Progesterone 100 mg
Combined Estradiol 0.5 mg / Progesterone 50 mg
Combined Estradiol 0.25 mg / Progesterone 50 mg
Placebo
Serious adverse events
| Measure |
Combined Estradiol 1 mg / Progesterone 100 mg
n=415 participants at risk
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=424 participants at risk
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=421 participants at risk
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=424 participants at risk
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=151 participants at risk
Two Placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Cardiac disorders
Cardiac Tamponade
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Cardiac disorders
Coronary Artery Disease
|
0.24%
1/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Cardiac disorders
Stress Cardiomyopothy
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Gastrointestinal disorders
Colitis Ischaemic
|
0.24%
1/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Gastrointestinal disorders
Colitis Ulcerative
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Gastrointestinal disorders
Gastroduodenal Haemorrhage
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Gastrointestinal disorders
Gastroduodenitis
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Gastrointestinal disorders
Pancreatitis
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Gastrointestinal disorders
Pancreatitis Acute
|
0.24%
1/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Gastrointestinal disorders
Small Intestinal Obstruction
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
General disorders
Non-Cardiac Chest Pain
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Hepatobiliary disorders
Hepatic Steatosis
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Immune system disorders
Angioedema
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Infections and infestations
Bronchitis
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Infections and infestations
Cholecystitis Infective
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.66%
1/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Infections and infestations
Clostridium Difficile Colitis
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Infections and infestations
Diverticulitis
|
0.48%
2/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Infections and infestations
Gastroenteritis Viral
|
0.24%
1/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Infections and infestations
Infectious Mononucleosis
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Infections and infestations
Pneumonia
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.47%
2/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Infections and infestations
Urosepsis
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Injury, poisoning and procedural complications
Ankle Fracture
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Injury, poisoning and procedural complications
Foot Fracture
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Injury, poisoning and procedural complications
Humerus Fracture
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Injury, poisoning and procedural complications
Incisional Hernia
|
0.24%
1/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Injury, poisoning and procedural complications
Jaw Fracture
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Injury, poisoning and procedural complications
Tibia Fracture
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Musculoskeletal and connective tissue disorders
Chondrocalcinosis Pyrophosphate
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Musculoskeletal and connective tissue disorders
Intervertebral Disc Protrusion
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Musculoskeletal and connective tissue disorders
Osteoarthritis
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Breast Cancer Female
|
0.48%
2/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Invasive Ductal Breast Carcinoma
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Lung Cancer Metastatic
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Myelodysplastic Syndrome
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Non-Small Cell Lung Cancer Stage IV
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Nervous system disorders
Balance Disorder
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Nervous system disorders
Cerebellar Infarction
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Nervous system disorders
Cerebrovascular Accident
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Nervous system disorders
Seizure
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Nervous system disorders
Subarachnoid Haemorrhage
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Psychiatric disorders
Psychotic Disorder
|
0.24%
1/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Reproductive system and breast disorders
Uterine Leiomyoma
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Reproductive system and breast disorders
Uterine Prolapse
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.66%
1/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Respiratory, thoracic and mediastinal disorders
Acute Respiratory Failure
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Respiratory, thoracic and mediastinal disorders
Chronic Obstructive Pulmonary Disease
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.47%
2/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Respiratory, thoracic and mediastinal disorders
Pleural Effusion
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Respiratory, thoracic and mediastinal disorders
Pneumonia Aspiration
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Vascular disorders
Aortic Aneurysm
|
0.24%
1/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Vascular disorders
Aortic Thrombosis
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Vascular disorders
Deep Vein Thrombosis
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Vascular disorders
Peripheral Arterial Occlusive Disease
|
0.00%
0/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.24%
1/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
Other adverse events
| Measure |
Combined Estradiol 1 mg / Progesterone 100 mg
n=415 participants at risk
Combined Estradiol 1 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 100 mg
n=424 participants at risk
Combined Estradiol 0.5 mg / Progesterone 100 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.5 mg / Progesterone 50 mg
n=421 participants at risk
Combined Estradiol 0.5 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Combined Estradiol 0.25 mg / Progesterone 50 mg
n=424 participants at risk
Combined Estradiol 0.25 mg / Progesterone 50 mg formulation and placebo softgel capsules taken orally once a day for twelve months.
|
Placebo
n=151 participants at risk
Two Placebo softgel capsules taken orally once a day for twelve months.
|
|---|---|---|---|---|---|
|
Nervous system disorders
Headache
|
7.5%
31/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
5.7%
24/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
10.7%
45/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
10.1%
43/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
2.6%
4/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Infections and infestations
Nasopharyngitis
|
6.0%
25/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
9.7%
41/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
8.8%
37/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
5.7%
24/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
2.6%
4/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Reproductive system and breast disorders
Breast Tenderness
|
10.8%
45/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
4.5%
19/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
5.9%
25/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
2.4%
10/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.66%
1/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Infections and infestations
Upper Respiratory Tract Infection
|
5.3%
22/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
6.1%
26/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
8.1%
34/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
3.5%
15/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
4.0%
6/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Gastrointestinal disorders
Nausea
|
4.8%
20/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
5.9%
25/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
4.5%
19/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
3.8%
16/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
1.3%
2/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Musculoskeletal and connective tissue disorders
Back Pain
|
5.3%
22/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
2.6%
11/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
3.6%
15/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
3.5%
15/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.66%
1/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Gastrointestinal disorders
Abdominal Pain
|
5.3%
22/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
2.4%
10/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
3.3%
14/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
3.5%
15/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
2.6%
4/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Infections and infestations
Sinusitis
|
4.8%
20/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
3.5%
15/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
3.1%
13/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
3.1%
13/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
2.0%
3/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Nervous system disorders
Dizziness
|
4.1%
17/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
3.5%
15/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
2.4%
10/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
1.9%
8/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
2.0%
3/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Reproductive system and breast disorders
Pelvic Pain
|
4.1%
17/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
3.5%
15/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
2.4%
10/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
1.7%
7/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.00%
0/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Gastrointestinal disorders
Diarrhoea
|
3.1%
13/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
3.1%
13/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
2.6%
11/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
2.6%
11/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
1.3%
2/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Infections and infestations
Vulvovaginal Mycotic Infection
|
3.4%
14/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
3.5%
15/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
3.3%
14/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
1.2%
5/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
2.6%
4/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Gastrointestinal disorders
Abdominal Distension
|
3.6%
15/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
1.4%
6/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
2.6%
11/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
2.6%
11/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.66%
1/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Reproductive system and breast disorders
Vaginal Discharge
|
3.9%
16/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
3.1%
13/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
1.7%
7/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
1.7%
7/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.66%
1/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Vascular disorders
Hypertension
|
1.7%
7/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
3.1%
13/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
2.1%
9/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
2.8%
12/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
1.3%
2/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Infections and infestations
Influenza
|
0.96%
4/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
1.4%
6/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
3.3%
14/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
2.8%
12/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
1.3%
2/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
|
Reproductive system and breast disorders
Vaginal Haemorrhage
|
3.4%
14/415 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
2.4%
10/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.71%
3/421 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
1.9%
8/424 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
0.66%
1/151 • Adverse Event data were collected on or after the subject signed Informed Consent through fifteen days following the last dose of Investigational Product. Treatment Emergent Adverse Event data were collected on or after the first dose of IP through fifteen days following the last dose of IP.
|
Additional Information
Sebastian Mirkin, MD, Chief Medical Officer
TherapeuticsMD
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place
Restriction type: GT60