Trial Outcomes & Findings for Dysport in the Treatment of Glabellar Lines in Chinese Subjects (NCT NCT02450526)
NCT ID: NCT02450526
Last Updated: 2019-08-06
Results Overview
At baseline (Cycle 1, Day 1) and at Cycle 1, Day 29, the Investigator assessed the appearance of the glabellar lines at maximum frown using a validated 4-point Photographic Scale of Glabellar Line Severity. This 4-point scale rated the severity of glabellar lines as Grade 0 (none), Grade 1 (mild), Grade 2 (moderate) and Grade 3 (severe). A responder was defined as having a severity grade of 0 or 1 at Cycle 1, Day 29, and a severity grade of 2 or 3 at maximum frown at baseline. Superiority analysis of active treatment versus placebo was carried out using a multivariate logistic regression model and adjusted for the stratification factors of gender and baseline severity score of glabellar lines at maximum frown measured by the ILA. The adjusted percentage of responders is presented for Cycle 1, Day 29.
COMPLETED
PHASE3
520 participants
At Cycle 1, Day 29.
2019-08-06
Participant Flow
This was a multicentre, phase III, randomised, double-blind (DB) then open-label (OL) study. The 12 month recruitment period began in April 2015. A total of 555 subjects were screened across the 10 study centres in China and 520 subjects were randomised into the study.
The 35 screen failures were due to 17 subjects not meeting the eligibility criteria, 17 subjects withdrawing consent, and one subject reporting an adverse event.
Participant milestones
| Measure |
Dysport® 50 Units (U) - DB Period
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 millilitres \[mL\]), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® 50 U - OL Period (Cycles 2-5)
After the first treatment cycle, all eligible subjects entered the OL period and received Dysport® 50 U (0.25 mL), injected into five predefined sites across the glabellar region. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites per treatment cycle.
Subjects received a maximum of four treatment cycles (Cycles 2 to 5) with Dysport®. These cycles occurred at intervals of no less than 84 days (12 weeks) between each cycle, depending upon individual duration of response to Dysport® treatment. Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study.
|
|---|---|---|---|---|---|
|
DB Period (Cycle 1)
STARTED
|
325
|
66
|
107
|
22
|
0
|
|
DB Period (Cycle 1)
Safety Population
|
326
|
66
|
107
|
21
|
0
|
|
DB Period (Cycle 1)
COMPLETED
|
294
|
63
|
97
|
20
|
0
|
|
DB Period (Cycle 1)
NOT COMPLETED
|
31
|
3
|
10
|
2
|
0
|
|
OL Period (Cycles 2-5)
STARTED
|
0
|
0
|
0
|
0
|
465
|
|
OL Period (Cycles 2-5)
Safety Population
|
0
|
0
|
0
|
0
|
465
|
|
OL Period (Cycles 2-5)
Discontinued During Cycle 2
|
0
|
0
|
0
|
0
|
28
|
|
OL Period (Cycles 2-5)
Discontinued During Cycle 3
|
0
|
0
|
0
|
0
|
11
|
|
OL Period (Cycles 2-5)
Discontinued During Cycle 4
|
0
|
0
|
0
|
0
|
2
|
|
OL Period (Cycles 2-5)
Discontinued During Cycle 5
|
0
|
0
|
0
|
0
|
0
|
|
OL Period (Cycles 2-5)
COMPLETED
|
0
|
0
|
0
|
0
|
424
|
|
OL Period (Cycles 2-5)
NOT COMPLETED
|
0
|
0
|
0
|
0
|
41
|
Reasons for withdrawal
| Measure |
Dysport® 50 Units (U) - DB Period
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 millilitres \[mL\]), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® 50 U - OL Period (Cycles 2-5)
After the first treatment cycle, all eligible subjects entered the OL period and received Dysport® 50 U (0.25 mL), injected into five predefined sites across the glabellar region. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites per treatment cycle.
Subjects received a maximum of four treatment cycles (Cycles 2 to 5) with Dysport®. These cycles occurred at intervals of no less than 84 days (12 weeks) between each cycle, depending upon individual duration of response to Dysport® treatment. Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study.
|
|---|---|---|---|---|---|
|
DB Period (Cycle 1)
Adverse Event
|
0
|
0
|
2
|
0
|
0
|
|
DB Period (Cycle 1)
Withdrawal by Subject
|
28
|
3
|
8
|
1
|
0
|
|
DB Period (Cycle 1)
Lost to Follow-up
|
1
|
0
|
0
|
0
|
0
|
|
DB Period (Cycle 1)
Protocol Violation
|
2
|
0
|
0
|
1
|
0
|
|
OL Period (Cycles 2-5)
Adverse Event
|
0
|
0
|
0
|
0
|
2
|
|
OL Period (Cycles 2-5)
Withdrawal by Subject
|
0
|
0
|
0
|
0
|
31
|
|
OL Period (Cycles 2-5)
Lack of Efficacy
|
0
|
0
|
0
|
0
|
1
|
|
OL Period (Cycles 2-5)
Protocol Violation
|
0
|
0
|
0
|
0
|
7
|
Baseline Characteristics
Dysport in the Treatment of Glabellar Lines in Chinese Subjects
Baseline characteristics by cohort
| Measure |
Dysport® 50 U - DB Period
n=325 Participants
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=66 Participants
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
n=107 Participants
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
n=22 Participants
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Total
n=520 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
|
|
Age, Categorical
Between 18 and 65 years
|
325 Participants
n=99 Participants
|
66 Participants
n=107 Participants
|
107 Participants
n=206 Participants
|
22 Participants
n=7 Participants
|
520 Participants
n=31 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
|
|
Age, Continuous
|
45.6 years
STANDARD_DEVIATION 9.4 • n=99 Participants
|
44.3 years
STANDARD_DEVIATION 9.5 • n=107 Participants
|
44.9 years
STANDARD_DEVIATION 8.2 • n=206 Participants
|
42.8 years
STANDARD_DEVIATION 9.8 • n=7 Participants
|
45.1 years
STANDARD_DEVIATION 9.2 • n=31 Participants
|
|
Sex: Female, Male
Female
|
282 Participants
n=99 Participants
|
57 Participants
n=107 Participants
|
94 Participants
n=206 Participants
|
19 Participants
n=7 Participants
|
452 Participants
n=31 Participants
|
|
Sex: Female, Male
Male
|
43 Participants
n=99 Participants
|
9 Participants
n=107 Participants
|
13 Participants
n=206 Participants
|
3 Participants
n=7 Participants
|
68 Participants
n=31 Participants
|
|
Race (NIH/OMB)
American Indian or Alaska Native
|
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
|
|
Race (NIH/OMB)
Asian
|
325 Participants
n=99 Participants
|
66 Participants
n=107 Participants
|
107 Participants
n=206 Participants
|
22 Participants
n=7 Participants
|
520 Participants
n=31 Participants
|
|
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
|
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
|
|
Race (NIH/OMB)
Black or African American
|
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
|
|
Race (NIH/OMB)
White
|
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
|
|
Race (NIH/OMB)
More than one race
|
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
|
|
Race (NIH/OMB)
Unknown or Not Reported
|
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
|
PRIMARY outcome
Timeframe: At Cycle 1, Day 29.Population: The modified Intent-to-treat (mITT) population was all randomised subjects who received study treatment in at least one injection site regardless of the amount administered and had both the baseline and Cycle 1, Day 29 assessments, for the ILA and subjects' self assessment (SSA) of glabellar lines at maximum frown.
At baseline (Cycle 1, Day 1) and at Cycle 1, Day 29, the Investigator assessed the appearance of the glabellar lines at maximum frown using a validated 4-point Photographic Scale of Glabellar Line Severity. This 4-point scale rated the severity of glabellar lines as Grade 0 (none), Grade 1 (mild), Grade 2 (moderate) and Grade 3 (severe). A responder was defined as having a severity grade of 0 or 1 at Cycle 1, Day 29, and a severity grade of 2 or 3 at maximum frown at baseline. Superiority analysis of active treatment versus placebo was carried out using a multivariate logistic regression model and adjusted for the stratification factors of gender and baseline severity score of glabellar lines at maximum frown measured by the ILA. The adjusted percentage of responders is presented for Cycle 1, Day 29.
Outcome measures
| Measure |
Dysport® 50 U - DB Period
n=294 Participants
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=60 Participants
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
n=94 Participants
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
n=19 Participants
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
|---|---|---|---|---|
|
Superiority Analysis of The Percentage of Responders Measured by the Investigator's Live Assessment (ILA) at Maximum Frown at Cycle 1, Day 29 (DB Period).
|
95.2 adjusted percentage of responders
Interval 91.2 to 97.4
|
0.9 adjusted percentage of responders
Interval 0.1 to 7.0
|
94.0 adjusted percentage of responders
Interval 85.2 to 97.7
|
4.3 adjusted percentage of responders
Interval 0.5 to 26.8
|
PRIMARY outcome
Timeframe: At Cycle 1, Day 29.Population: The mITT population was all randomised subjects who received study treatment in at least one injection site regardless of the amount administered and had both the baseline and Cycle 1, Day 29 assessments, for the ILA and SSA of glabellar lines at maximum frown.
At baseline (Cycle 1, Day 1) and at Cycle 1, Day 29, subjects assessed the appearance of their glabellar lines at maximum frown using a 4-point categorical scale. The 4-point scale represents the severity of glabellar lines as Grade 0 (no wrinkles), Grade 1 (mild wrinkles), Grade 2 (moderate wrinkles) and Grade 3 (severe wrinkles). For the SSA, a responder was defined as having a severity grade of 0 or 1 at maximum frown at Cycle 1, Day 29, and a severity grade of 2 or 3 at maximum frown at baseline. Superiority analysis of active treatment versus placebo was carried out using a multivariate logistic regression model and adjusted for the stratification factors of gender and baseline severity score of glabellar lines at maximum frown measured by the ILA. The adjusted percentage of responders is presented for Cycle 1, Day 29.
Outcome measures
| Measure |
Dysport® 50 U - DB Period
n=294 Participants
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=60 Participants
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
n=94 Participants
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
n=19 Participants
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
|---|---|---|---|---|
|
Superiority Analysis of The Percentage of Responders Measured by the SSA at Maximum Frown at Cycle 1, Day 29 (DB Period).
|
89.4 adjusted percentage of responders
Interval 84.4 to 93.0
|
1.9 adjusted percentage of responders
Interval 0.4 to 8.4
|
89.3 adjusted percentage of responders
Interval 79.2 to 94.9
|
1.5 adjusted percentage of responders
Interval 0.1 to 21.0
|
PRIMARY outcome
Timeframe: At Cycle 1, Day 29.Population: The mITT population was all randomised subjects who received study treatment in at least one injection site regardless of the amount administered and had both the baseline and Cycle 1, Day 29 assessments, for the ILA and SSA of glabellar lines at maximum frown.
At baseline (Cycle 1, Day 1) and at Cycle 1, Day 29, the Investigator assessed the appearance of the glabellar lines at maximum frown using a validated 4-point Photographic Scale of Glabellar Line Severity. This 4-point scale rated the severity of glabellar lines as Grade 0 (none), Grade 1 (mild), Grade 2 (moderate) and Grade 3 (severe). A responder was defined as having a severity grade of 0 or 1 at Cycle 1, Day 29, and a severity grade of 2 or 3 at maximum frown at baseline. Non Inferiority analysis of Dysport® versus Botox was carried out using a multivariate logistic regression model and adjusted for the stratification factors of gender and baseline severity score of glabellar lines at maximum frown measured by the ILA. The adjusted percentage of responders is presented for Cycle 1, Day 29.
Outcome measures
| Measure |
Dysport® 50 U - DB Period
n=294 Participants
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=94 Participants
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
|---|---|---|---|---|
|
Non-Inferiority Analysis of The Percentage of Responders Measured by the Investigator's Live Assessment (ILA) at Maximum Frown at Cycle 1, Day 29 (DB Period).
|
94.7 adjusted percentage of responders
Interval 90.8 to 96.9
|
97.0 adjusted percentage of responders
Interval 92.0 to 98.9
|
—
|
—
|
SECONDARY outcome
Timeframe: At Cycle 1, Day 29.Population: The mITT population was all randomised subjects who received study treatment in at least one injection site regardless of the amount administered and had both the baseline and Cycle 1, Day 29 assessments, for the ILA and SSA of glabellar lines at maximum frown. Subjects with a baseline score of 0 or 1 are excluded from the analysis.
Photographs of the glabellar region of subjects were taken at maximum frown at baseline (Cycle 1, Day 1) and at Cycle 1, Day 29. Photographs were assessed by an Independent Experts Committee using a validated 4-point Photographic Scale of Glabellar Line Severity which rated the severity of glabellar lines as Grade 0 (none), Grade 1 (mild), Grade 2 (moderate) and Grade 3 (severe). The median of three readings by three independent reviewers was used in the analysis. A responder was defined as having a severity grade of 0 or 1 at Cycle 1, Day 29, and a severity grade of 2 or 3 at baseline. Superiority analysis of active treatment to placebo was carried out using a multivariate logistic regression model and adjusted for the stratification factors of gender and baseline severity score of glabellar lines at maximum frown measured by the ILA. The adjusted percentage of responders is presented for Cycle 1, Day 29.
Outcome measures
| Measure |
Dysport® 50 U - DB Period
n=194 Participants
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=34 Participants
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
n=60 Participants
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
n=11 Participants
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
|---|---|---|---|---|
|
The Percentage of Responders With Respect to Independent Reviewer's Assessment of Photographs of the Subject's Glabellar Lines at Maximum Frown at Cycle 1, Day 29 (DB Period).
|
99.1 adjusted percentage of responders
Interval 95.0 to 99.8
|
25.3 adjusted percentage of responders
Interval 11.6 to 46.7
|
94.4 adjusted percentage of responders
Interval 85.0 to 98.1
|
31.5 adjusted percentage of responders
Interval 9.4 to 67.1
|
SECONDARY outcome
Timeframe: At Cycle 1, Day 29.Population: The mITT population was all randomised subjects who received study treatment in at least one injection site regardless of the amount administered and had both the baseline and Cycle 1, Day 29 assessments, for the ILA and SSA of glabellar lines at maximum frown.
On Cycle 1, Day 29, subjects were asked to assess the change, since the last treatment administration, in the appearance of their glabellar lines using the following 9-point Global Assessment Scale: +4 =100% improvement; +3 =75% improvement; +2 =50% improvement; +1 =25% improvement; 0 =no change; -1 =25% worsening; -2 =50%worsening; -3 =75% worsening; -4 =100% worsening. The mean SGA score at Cycle 1, Day 29 is presented.
Outcome measures
| Measure |
Dysport® 50 U - DB Period
n=294 Participants
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=60 Participants
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
n=94 Participants
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
n=19 Participants
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
|---|---|---|---|---|
|
Mean Subject's Global Assessment (SGA) Score at Cycle 1, Day 29 (DB Period).
|
2.6 units on the SGA scale
Standard Deviation 1.1
|
0.1 units on the SGA scale
Standard Deviation 0.4
|
2.7 units on the SGA scale
Standard Deviation 1.1
|
0.1 units on the SGA scale
Standard Deviation 0.3
|
SECONDARY outcome
Timeframe: At Cycle 1, Day 29.Population: The mITT population was all randomised subjects who received study treatment in at least one injection site regardless of the amount administered and had both the baseline and Cycle 1, Day 29 assessments, for the ILA and SSA of glabellar lines at maximum frown.
On Cycle 1, Day 29, subjects were asked to assess the change, since the last treatment administration, in the appearance of their glabellar lines using the following 9-point Global Assessment Scale: +4 =100% improvement; +3 =75% improvement; +2 =50% improvement; +1 =25% improvement; 0 =no change; -1 =25% worsening; -2 =50% worsening; -3 =75% worsening; -4 =100% worsening. A responder, based on the SGA scale, was defined as having a grade of at least +2 (50% improvement). Superiority analysis of active treatment versus placebo was carried out using a multivariate logistic regression model and adjusted for the stratification factors of gender and baseline severity score of glabellar lines at maximum frown measured by the ILA. The adjusted percentage of responders is presented for Cycle 1, Day 29.
Outcome measures
| Measure |
Dysport® 50 U - DB Period
n=294 Participants
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=60 Participants
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
n=94 Participants
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
n=19 Participants
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
|---|---|---|---|---|
|
The Percentage of Responders With Respect to the SGA Score at Cycle 1, Day 29 (DB Period).
|
85.1 adjusted percentage of responders
Interval 80.2 to 88.9
|
1.3 adjusted percentage of responders
Interval 0.2 to 9.0
|
85.2 adjusted percentage of responders
Interval 74.4 to 91.9
|
2.4 adjusted percentage of responders
Interval 0.2 to 23.3
|
OTHER_PRE_SPECIFIED outcome
Timeframe: Up to Cycle 1, Day 85.Population: The mITT population was all randomised subjects who received study treatment in at least one injection site regardless of the amount administered and had both the baseline and Cycle 1, Day 29 assessments, for the ILA and SSA of glabellar lines at maximum frown. Only subjects with data available for analysis at each time point are presented.
At baseline (Cycle 1, Day 1) and at all subsequent study visits, the Investigator assessed the appearance of the glabellar lines at maximum frown using a validated 4-point photographic scale of glabellar line severity. This 4-point scale rated the severity of glabellar lines as Grade 0 (none), Grade 1 (mild), Grade 2 (moderate) and Grade 3 (severe). A responder was defined as having a severity grade of 0 or 1 at any given visit, and a severity grade of 2 or 3 at baseline. Superiority analysis of active treatment versus placebo was carried out using a multivariate logistic regression model and adjusted for the stratification factors of gender and baseline severity score of glabellar lines at maximum frown measured by the ILA. The adjusted percentage of responders is presented for all visits up to Day 85 in the DB period (except Cycle 1, Day 29).
Outcome measures
| Measure |
Dysport® 50 U - DB Period
n=294 Participants
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=60 Participants
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
n=94 Participants
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
n=19 Participants
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
|---|---|---|---|---|
|
The Percentage of Responders Measured by the ILA at Maximum Frown at Cycle 1 Study Visits (DB Period).
Cycle 1, Day 8
|
86.3 adjusted percentage of responders
Interval 81.0 to 90.3
|
1.0 adjusted percentage of responders
Interval 0.1 to 6.9
|
87.3 adjusted percentage of responders
Interval 76.1 to 93.7
|
1.1 adjusted percentage of responders
Interval 0.1 to 18.4
|
|
The Percentage of Responders Measured by the ILA at Maximum Frown at Cycle 1 Study Visits (DB Period).
Cycle 1, Day 57
|
87.7 adjusted percentage of responders
Interval 82.7 to 91.4
|
2.9 adjusted percentage of responders
Interval 0.8 to 9.7
|
92.6 adjusted percentage of responders
Interval 79.4 to 97.6
|
1.0 adjusted percentage of responders
Interval 0.0 to 20.7
|
|
The Percentage of Responders Measured by the ILA at Maximum Frown at Cycle 1 Study Visits (DB Period).
Cycle 1, Day 85
|
80.3 adjusted percentage of responders
Interval 72.1 to 86.6
|
0.1 adjusted percentage of responders
Interval 0.0 to 3.2
|
76.4 adjusted percentage of responders
Interval 63.8 to 85.6
|
1.1 adjusted percentage of responders
Interval 0.0 to 22.4
|
OTHER_PRE_SPECIFIED outcome
Timeframe: Up to Cycle 1, Day 85.Population: The mITT population was all randomised subjects who received study treatment in at least one injection site regardless of the amount administered and had both the baseline and Cycle 1, Day 29 assessments, for the ILA and SSA of glabellar lines at maximum frown.
At baseline (Cycle 1, Day 1) and all subsequent study visits, subjects assessed the appearance of their glabellar lines at maximum frown using a 4-point categorical scale. The 4-point scale represents the severity of glabellar lines as Grade 0 (no wrinkles), Grade 1 (mild wrinkles), Grade 2 (moderate wrinkles) and Grade 3 (severe wrinkles). For the SSA, a responder was defined as having a severity grade of 0 or 1 at maximum frown at any given visit, and a severity grade of 2 or 3 at maximum frown at baseline. Superiority analysis of active treatment versus placebo was carried out using a multivariate logistic regression model and adjusted for the stratification factors of gender and baseline severity score of glabellar lines at maximum frown measured by the ILA. The adjusted percentage of responders is presented for all visits up to Day 85 in the DB period (except Cycle 1, Day 29).
Outcome measures
| Measure |
Dysport® 50 U - DB Period
n=294 Participants
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=60 Participants
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
n=94 Participants
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
n=19 Participants
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
|---|---|---|---|---|
|
The Percentage of Responders Measured by the SSA at Maximum Frown at Cycle 1 Study Visits (DB Period).
Cycle 1, Day 8
|
78.6 adjusted percentage of responders
Interval 72.7 to 83.5
|
2.0 adjusted percentage of responders
Interval 0.5 to 8.5
|
77.3 adjusted percentage of responders
Interval 66.4 to 85.5
|
7.4 adjusted percentage of responders
Interval 1.5 to 29.8
|
|
The Percentage of Responders Measured by the SSA at Maximum Frown at Cycle 1 Study Visits (DB Period).
Cycle 1, Day 57
|
84.9 adjusted percentage of responders
Interval 79.6 to 89.0
|
2.1 adjusted percentage of responders
Interval 0.5 to 8.7
|
88.1 adjusted percentage of responders
Interval 76.8 to 94.4
|
2.6 adjusted percentage of responders
Interval 0.2 to 23.5
|
|
The Percentage of Responders Measured by the SSA at Maximum Frown at Cycle 1 Study Visits (DB Period).
Cycle 1, Day 85
|
68.2 adjusted percentage of responders
Interval 61.5 to 74.2
|
1.7 adjusted percentage of responders
Interval 0.4 to 7.1
|
72.2 adjusted percentage of responders
Interval 59.4 to 82.3
|
1.0 adjusted percentage of responders
Interval 0.0 to 21.5
|
OTHER_PRE_SPECIFIED outcome
Timeframe: Up to Cycle 1, Day 85.Population: The mITT population was all randomised subjects who received study treatment in at least one injection site regardless of the amount administered and had both the baseline and Cycle 1, Day 29 assessments, for the ILA and SSA of glabellar lines at maximum frown. Subjects with a baseline score of 0 or 1 were excluded from the analysis of responders.
At baseline (Cycle 1, Day 1) and at all subsequent study visits, the Investigator assessed the appearance of the glabellar lines at rest using a validated 4-point photographic scale of glabellar line severity. This 4-point scale rated the severity of glabellar lines as Grade 0 (none), Grade 1 (mild), Grade 2 (moderate) and Grade 3 (severe). A responder was defined as having a severity grade of 0 or 1 at rest at any given visit, and a severity grade of 2 or 3 at rest at baseline. Superiority analysis of active treatment versus placebo was carried out using a multivariate logistic regression model and adjusted for the stratification factors of gender and baseline severity score of glabellar lines at maximum frown measured by the ILA. The adjusted percentage of responders is presented for all visits up to Day 85 in the DB period (except Cycle 1, Day 29).
Outcome measures
| Measure |
Dysport® 50 U - DB Period
n=123 Participants
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=17 Participants
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
n=33 Participants
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
n=3 Participants
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
|---|---|---|---|---|
|
The Percentage of Responders Measured by the ILA at Rest at Cycle 1 Study Visits (DB Period).
Cycle 1, Day 8
|
54.2 adjusted percentage of responders
Interval 44.4 to 63.6
|
12.2 adjusted percentage of responders
Interval 2.8 to 39.6
|
65.4 adjusted percentage of responders
Interval 44.4 to 81.7
|
8.4 adjusted percentage of responders
Interval 0.2 to 82.2
|
|
The Percentage of Responders Measured by the ILA at Rest at Cycle 1 Study Visits (DB Period).
Cycle 1, Day 57
|
66.5 adjusted percentage of responders
Interval 55.6 to 75.9
|
13.1 adjusted percentage of responders
Interval 3.2 to 40.5
|
68.2 adjusted percentage of responders
Interval 47.3 to 83.7
|
24.9 adjusted percentage of responders
Interval 1.5 to 87.7
|
|
The Percentage of Responders Measured by the ILA at Rest at Cycle 1 Study Visits (DB Period).
Cycle 1, Day 85
|
61.8 adjusted percentage of responders
Interval 51.1 to 71.4
|
22.1 adjusted percentage of responders
Interval 7.4 to 50.1
|
71.8 adjusted percentage of responders
Interval 49.3 to 87.0
|
5.8 adjusted percentage of responders
Interval 0.1 to 75.0
|
OTHER_PRE_SPECIFIED outcome
Timeframe: At Cycle 1, Day 85.Population: The mITT population was all randomised subjects who received study treatment in at least one injection site regardless of the amount administered and had both the baseline and Cycle 1, Day 29 assessments, for the ILA and SSA of glabellar lines at maximum frown. Subjects with a baseline score of 0 or 1 were excluded from the analysis.
Photographs of the glabellar region of subjects were taken at baseline and at maximum frown at Cycle 1, Day 85. Photographs were assessed by an Independent Experts Committee using a validated 4-point Photographic Scale of Glabellar Line Severity. This 4-point scale rated the severity of glabellar lines as Grade 0 (none), Grade 1 (mild), Grade 2 (moderate) and Grade 3 (severe). The median of 3 readings by 3 independent reviewers was used in the analysis. A responder was defined as having a severity grade of 0 or 1 at Cycle 1, Day 85, and a severity grade of 2 or 3 at baseline. Superiority analysis of active treatment versus placebo was carried out using a multivariate logistic regression model and adjusted for the stratification factors of gender and baseline severity score of glabellar lines at maximum frown measured by the ILA. The adjusted percentage of responders is presented for Cycle 1, Day 85 .
Outcome measures
| Measure |
Dysport® 50 U - DB Period
n=294 Participants
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=60 Participants
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
n=94 Participants
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
n=19 Participants
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
|---|---|---|---|---|
|
The Percentage of Responders With Respect to Independent Reviewer's Assessment of Photographs of the Subject's Glabellar Lines at Maximum Frown at Cycle 1, Day 85 (DB Period).
|
93.3 adjusted percentage of responders
Interval 87.4 to 96.5
|
13.5 adjusted percentage of responders
Interval 5.1 to 30.9
|
89.0 adjusted percentage of responders
Interval 74.5 to 95.7
|
22.0 adjusted percentage of responders
Interval 5.6 to 57.0
|
OTHER_PRE_SPECIFIED outcome
Timeframe: Up to Cycle 1, Day 85.Population: The mITT population was all randomised subjects who received study treatment in at least one injection site regardless of the amount administered and had both the baseline and Cycle 1, Day 29 assessments, for the ILA and SSA of glabellar lines at maximum frown. Only subjects with data available for analysis at each time point are presented.
On all study visits, subjects were asked to assess the change, since the last treatment administration, in the appearance of their glabellar lines using the following 9-point Global Assessment Scale: +4 =100% improvement; +3 =75% improvement; +2 =50% improvement; +1 =25% improvement; 0 =no change; -1 =25% worsening; -2 =50% worsening; -3 =75% worsening; -4 =100% worsening. The mean SGA score for study visits on Day 8 to Day 85 in the DB period is presented (except Cycle 1, Day 29).
Outcome measures
| Measure |
Dysport® 50 U - DB Period
n=294 Participants
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=60 Participants
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
n=94 Participants
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
n=19 Participants
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
|---|---|---|---|---|
|
Mean SGA Score at Cycle 1 Study Visits (DB Period).
Cycle 1, Day 85
|
1.9 units on the SGA scale
Standard Deviation 1.3
|
0.1 units on the SGA scale
Standard Deviation 0.6
|
1.8 units on the SGA scale
Standard Deviation 1.2
|
0.1 units on the SGA scale
Standard Deviation 0.2
|
|
Mean SGA Score at Cycle 1 Study Visits (DB Period).
Cycle 1, Day 8
|
2.3 units on the SGA scale
Standard Deviation 1.2
|
0.1 units on the SGA scale
Standard Deviation 0.4
|
2.3 units on the SGA scale
Standard Deviation 1.3
|
0.2 units on the SGA scale
Standard Deviation 0.5
|
|
Mean SGA Score at Cycle 1 Study Visits (DB Period).
Cycle 1, Day 57
|
2.4 units on the SGA scale
Standard Deviation 1.2
|
0.1 units on the SGA scale
Standard Deviation 0.6
|
2.4 units on the SGA scale
Standard Deviation 1.1
|
0.1 units on the SGA scale
Standard Deviation 0.4
|
OTHER_PRE_SPECIFIED outcome
Timeframe: Up to Cycle 1, Day 85.Population: The mITT population was all randomised subjects who received study treatment in at least one injection site regardless of the amount administered and had both the baseline and Cycle 1, Day 29 assessments, for the ILA and SSA of glabellar lines at maximum frown. Only subjects with data available for analysis at each time point are presented.
On all study visits, subjects were asked to assess the change, since the last treatment administration, in the appearance of their glabellar lines using the following 9-point Global Assessment Scale: +4 =100% improvement; +3 =75% improvement; +2 =50% improvement; +1 =25% improvement; 0 =no change; -1 =25% worsening; -2 =50%worsening; -3 =75% worsening; -4 =100% worsening. A responder, based on the SGA scale, was defined as having a grade of at least +2 (50% improvement). Superiority analysis of active treatment versus placebo was carried out using a multivariate logistic regression model and adjusted for the stratification factors of gender and baseline severity score of glabellar lines at maximum frown measured by the ILA. The adjusted percentage of responders is presented for all visits up to Day 85 in the DB period (except Cycle 1, Day 29).
Outcome measures
| Measure |
Dysport® 50 U - DB Period
n=294 Participants
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=60 Participants
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
n=94 Participants
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
n=19 Participants
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
|---|---|---|---|---|
|
The Percentage of Responders With Respect to the SGA Score at Cycle 1 Study Visits (DB Period).
Cycle 1, Day 8
|
78.0 adjusted percentage of responders
Interval 72.3 to 82.7
|
1.2 adjusted percentage of responders
Interval 0.2 to 8.5
|
73.7 adjusted percentage of responders
Interval 62.5 to 82.5
|
2.8 adjusted percentage of responders
Interval 0.3 to 22.8
|
|
The Percentage of Responders With Respect to the SGA Score at Cycle 1 Study Visits (DB Period).
Cycle 1, Day 57
|
80.1 adjusted percentage of responders
Interval 74.4 to 84.7
|
3.4 adjusted percentage of responders
Interval 1.0 to 10.7
|
79.5 adjusted percentage of responders
Interval 67.8 to 87.8
|
1.8 adjusted percentage of responders
Interval 0.1 to 22.2
|
|
The Percentage of Responders With Respect to the SGA Score at Cycle 1 Study Visits (DB Period).
Cycle 1, Day 85
|
65.2 adjusted percentage of responders
Interval 59.1 to 70.9
|
2.5 adjusted percentage of responders
Interval 0.6 to 9.7
|
57.4 adjusted percentage of responders
Interval 46.5 to 67.5
|
2.0 adjusted percentage of responders
Interval 0.1 to 23.5
|
OTHER_PRE_SPECIFIED outcome
Timeframe: Up to Cycle 1, Day 85.Population: The mITT population was all randomised subjects who received study treatment in at least one injection site regardless of the amount administered and had both the baseline and Cycle 1, Day 29 assessments, for the ILA and SSA of glabellar lines at maximum frown. Only subjects with data available for analysis at each time point is presented.
At baseline (Cycle 1, Day 1) and all subsequent study visits in Cycle 1, subjects were asked to evaluate their age over the past 7 days at the time of assessment, using the following categories: * I look like my current age; * I look \_ years younger; * I look \_ years older. The LS mean change from baseline in subject's self-perception of age at all study visits in the DB Period was calculated. A negative LS mean change from baseline in the subject's self-perception of age indicates that the subject's self-perception was to look younger compared with baseline.
Outcome measures
| Measure |
Dysport® 50 U - DB Period
n=294 Participants
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=60 Participants
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
n=94 Participants
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
n=19 Participants
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
|---|---|---|---|---|
|
Least Squares (LS) Mean Change From Baseline in Subject's Self-perception of Age at Cycle 1 Study Visits (DB Period).
Cycle 1, Day 8
|
-2.083 years
Standard Error 0.278
|
0.344 years
Standard Error 0.471
|
-1.442 years
Standard Error 0.422
|
-0.266 years
Standard Error 0.710
|
|
Least Squares (LS) Mean Change From Baseline in Subject's Self-perception of Age at Cycle 1 Study Visits (DB Period).
Cycle 1, Day 29
|
-2.566 years
Standard Error 0.296
|
0.478 years
Standard Error 0.524
|
-2.421 years
Standard Error 0.437
|
-0.003 years
Standard Error 0.754
|
|
Least Squares (LS) Mean Change From Baseline in Subject's Self-perception of Age at Cycle 1 Study Visits (DB Period).
Cycle 1, Day 57
|
-2.483 years
Standard Error 0.293
|
0.698 years
Standard Error 0.515
|
-1.857 years
Standard Error 0.420
|
-0.453 years
Standard Error 0.711
|
|
Least Squares (LS) Mean Change From Baseline in Subject's Self-perception of Age at Cycle 1 Study Visits (DB Period).
Cycle 1, Day 85
|
-2.035 years
Standard Error 0.281
|
0.581 years
Standard Error 0.481
|
-1.374 years
Standard Error 0.452
|
-0.208 years
Standard Error 0.802
|
OTHER_PRE_SPECIFIED outcome
Timeframe: At Cycle 1, Day 8.Population: The mITT population was all randomised subjects who received study treatment in at least one injection site regardless of the amount administered and had both the baseline and Cycle 1, Day 29 assessments, for the ILA and SSA of glabellar lines at maximum frown. Only subjects with treatment response on Cycle 1, Day 8 were analysed.
Subjects were given the diary card at baseline (Cycle 1, Day 1 ) and asked to record their assessment of study treatment response for the first 7 days post-treatment (Days 2 to 8). They were asked to respond 'yes' or 'no' to the following question: 'Since being injected have you noticed an improvement in the appearance of your glabellar lines (lines between your eyebrows)?' Subjects with no treatment response were censored at the date of last assessment of treatment response recorded in the diary card. The 50th percentile of Kaplan-Meier estimates was used to estimate the median time to onset of treatment response for each treatment group.
Outcome measures
| Measure |
Dysport® 50 U - DB Period
n=268 Participants
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=8 Participants
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
n=82 Participants
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
n=5 Participants
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
|---|---|---|---|---|
|
The Time to Onset of Treatment Response Based on the Subject's Diary Card (DB Period).
|
2.0 days
Interval 2.0 to 3.0
|
NA days
Results were non-calculable due to censored data.
|
3.0 days
Interval 2.0 to 3.0
|
NA days
Interval 7.0 to
Results were non-calculable due to censored data.
|
OTHER_PRE_SPECIFIED outcome
Timeframe: Up to Cycle 5, Day 85.Population: The OL population was all randomised subjects who received any dose of OL Dysport®. Only subjects with data available for analysis at each time point are presented.
At baseline (Cycle 1, Day 1) and all subsequent study visits (per treatment cycle) in the OL period, the Investigator assessed the appearance of the glabellar lines at maximum frown using a validated 4-point Photographic Scale of Glabellar Line Severity. This 4-point scale rated the severity of glabellar lines as Grade 0 (none), Grade 1 (mild), Grade 2 (moderate) and Grade 3 (severe). A responder was defined as having a severity grade of 0 or 1 at each study visit, and a severity grade of 2 or 3 at baseline. The proportion (percentage) of responders measured by ILA at all study visits in each treatment cycle, is presented.
Outcome measures
| Measure |
Dysport® 50 U - DB Period
n=424 Participants
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=355 Participants
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
n=232 Participants
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
n=98 Participants
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
|---|---|---|---|---|
|
The Percentage of Responders Measured by the ILA at Maximum Frown at All Other Study Visits (OL Period).
Day 8
|
92.9 percentage of responders
Interval 90.1 to 95.2
|
92.1 percentage of responders
Interval 88.8 to 94.7
|
92.2 percentage of responders
Interval 88.0 to 95.3
|
84.7 percentage of responders
Interval 76.0 to 91.2
|
|
The Percentage of Responders Measured by the ILA at Maximum Frown at All Other Study Visits (OL Period).
Day 29
|
92.7 percentage of responders
Interval 89.8 to 95.0
|
93.5 percentage of responders
Interval 90.4 to 95.8
|
90.1 percentage of responders
Interval 85.5 to 93.6
|
84.7 percentage of responders
Interval 76.0 to 91.2
|
|
The Percentage of Responders Measured by the ILA at Maximum Frown at All Other Study Visits (OL Period).
Day 57
|
88.0 percentage of responders
Interval 84.5 to 90.9
|
88.7 percentage of responders
Interval 85.0 to 91.8
|
85.8 percentage of responders
Interval 80.6 to 90.0
|
81.6 percentage of responders
Interval 72.5 to 88.7
|
|
The Percentage of Responders Measured by the ILA at Maximum Frown at All Other Study Visits (OL Period).
Day 85
|
71.7 percentage of responders
Interval 67.2 to 75.9
|
73.8 percentage of responders
Interval 68.9 to 78.3
|
68.1 percentage of responders
Interval 61.7 to 74.1
|
61.2 percentage of responders
Interval 50.8 to 70.9
|
OTHER_PRE_SPECIFIED outcome
Timeframe: Up to Cycle 5, Day 85.Population: The OL population was all randomised subjects who received any dose of OL Dysport®. Only subjects with data available for analysis at each time point are presented.
At baseline (Cycle 1, Day 1) and all subsequent study visits per treatment cycle in the OL period, subjects assessed the appearance of their glabellar lines at maximum frown using a 4-point categorical scale. The 4-point scale represents the severity of glabellar lines as Grade 0 (no wrinkles), Grade 1 (mild wrinkles), Grade 2 (moderate wrinkles) and Grade 3 (severe wrinkles). For the SSA, a responder was defined as having a severity grade of no wrinkles (0) or mild wrinkles (1) at maximum frown at a given visit and a severity grade of moderate wrinkles (2) or severe wrinkles (3) at maximum frown at baseline. The proportion (percentage) of responders measured by SSA at all study visits in Cycle 2 to 5 is presented.
Outcome measures
| Measure |
Dysport® 50 U - DB Period
n=424 Participants
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=355 Participants
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
n=232 Participants
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
n=98 Participants
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
|---|---|---|---|---|
|
The Percentage of Responders Measured by the SSA at Maximum Frown at All Other Study Visits (OL Period).
Day 8
|
85.3 percentage of responders
Interval 81.6 to 88.6
|
89.0 percentage of responders
Interval 85.3 to 92.1
|
87.5 percentage of responders
Interval 82.5 to 91.5
|
77.6 percentage of responders
Interval 68.0 to 85.4
|
|
The Percentage of Responders Measured by the SSA at Maximum Frown at All Other Study Visits (OL Period).
Day 29
|
89.1 percentage of responders
Interval 85.8 to 91.9
|
88.5 percentage of responders
Interval 84.7 to 91.6
|
87.5 percentage of responders
Interval 82.5 to 91.5
|
77.6 percentage of responders
Interval 68.0 to 85.4
|
|
The Percentage of Responders Measured by the SSA at Maximum Frown at All Other Study Visits (OL Period).
Day 57
|
85.1 percentage of responders
Interval 81.4 to 88.4
|
83.9 percentage of responders
Interval 79.7 to 87.6
|
82.8 percentage of responders
Interval 77.3 to 87.4
|
71.4 percentage of responders
Interval 61.4 to 80.1
|
|
The Percentage of Responders Measured by the SSA at Maximum Frown at All Other Study Visits (OL Period).
Day 85
|
68.8 percentage of responders
Interval 64.1 to 73.2
|
70.7 percentage of responders
Interval 65.7 to 75.4
|
62.5 percentage of responders
Interval 55.9 to 68.7
|
62.2 percentage of responders
Interval 51.9 to 71.8
|
OTHER_PRE_SPECIFIED outcome
Timeframe: Up to Cycle 5, Day 85.Population: The OL population was all randomised subjects who received any dose of OL Dysport®. Only subjects with a baseline score of 2 or 3 and with data available for analysis at each time point are presented.
At baseline (Cycle 1, Day 1) and all subsequent study visits per treatment cycle in the OL period, the Investigator assessed the appearance of the glabellar lines at rest using a validated 4-point Photographic Scale of Glabellar Line Severity. This 4-point scale rated the severity of glabellar lines as Grade 0 (none), Grade 1 (mild), Grade 2 (moderate) and Grade 3 (severe). A responder was defined as having a severity grade of 0 or 1 at a given visit, and a severity grade of 2 or 3 at baseline. Subjects with a baseline score of 0 or 1 were excluded from the analysis of responders. The proportion (percentage) of responders measured by ILA at all study visits per treatment cycle in in the OL period is presented.
Outcome measures
| Measure |
Dysport® 50 U - DB Period
n=109 Participants
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=69 Participants
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
n=44 Participants
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
n=16 Participants
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
|---|---|---|---|---|
|
The Percentage of Responders Measured by the ILA at Rest at All Study Visits (OL Period).
Day 8
|
60.6 percentage of responders
Interval 50.7 to 69.8
|
52.2 percentage of responders
Interval 39.8 to 64.4
|
54.5 percentage of responders
Interval 38.8 to 69.6
|
18.8 percentage of responders
Interval 4.0 to 45.6
|
|
The Percentage of Responders Measured by the ILA at Rest at All Study Visits (OL Period).
Day 29
|
63.3 percentage of responders
Interval 53.5 to 72.3
|
58.0 percentage of responders
Interval 45.5 to 69.8
|
54.5 percentage of responders
Interval 38.8 to 69.6
|
25.0 percentage of responders
Interval 7.3 to 52.4
|
|
The Percentage of Responders Measured by the ILA at Rest at All Study Visits (OL Period).
Day 57
|
62.4 percentage of responders
Interval 52.6 to 71.5
|
56.5 percentage of responders
Interval 44.0 to 68.4
|
54.5 percentage of responders
Interval 38.8 to 69.6
|
25.0 percentage of responders
Interval 7.3 to 52.4
|
|
The Percentage of Responders Measured by the ILA at Rest at All Study Visits (OL Period).
Day 85
|
56.9 percentage of responders
Interval 47.0 to 66.3
|
58.0 percentage of responders
Interval 45.5 to 69.8
|
59.1 percentage of responders
Interval 43.2 to 73.7
|
25.0 percentage of responders
Interval 7.3 to 52.4
|
OTHER_PRE_SPECIFIED outcome
Timeframe: Up to Cycle 5, Day 85.Population: The OL population was all randomised subjects who received any dose of OL Dysport®. Only subjects with data available for analysis at each time point are presented.
On each study visit per treatment cycle in the OL period, subjects were asked to assess the change, since the last treatment administration, in the appearance of their glabellar lines using the following 9-point Global Assessment Scale: +4 =100% improvement; +3 =75% improvement; +2 =50% improvement; +1 =25% improvement; 0 =no change; -1 =25% worsening; -2 =50%worsening; -3 =75% worsening; -4 =100% worsening. The mean SGA score for study visits on Day 8 to Day 85 in the OL period is presented.
Outcome measures
| Measure |
Dysport® 50 U - DB Period
n=424 Participants
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=355 Participants
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
n=232 Participants
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
n=98 Participants
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
|---|---|---|---|---|
|
Mean SGA Score at All Other Study Visits (OL Period).
Day 8
|
2.5 units on the SGA scale
Standard Deviation 1.1
|
2.4 units on the SGA scale
Standard Deviation 1.1
|
2.5 units on the SGA scale
Standard Deviation 1.2
|
2.1 units on the SGA scale
Standard Deviation 1.1
|
|
Mean SGA Score at All Other Study Visits (OL Period).
Day 29
|
2.6 units on the SGA scale
Standard Deviation 1.1
|
2.5 units on the SGA scale
Standard Deviation 1.0
|
2.4 units on the SGA scale
Standard Deviation 1.1
|
2.1 units on the SGA scale
Standard Deviation 1.2
|
|
Mean SGA Score at All Other Study Visits (OL Period).
Day 57
|
2.4 units on the SGA scale
Standard Deviation 1.1
|
2.3 units on the SGA scale
Standard Deviation 1.2
|
2.2 units on the SGA scale
Standard Deviation 1.1
|
1.9 units on the SGA scale
Standard Deviation 1.1
|
|
Mean SGA Score at All Other Study Visits (OL Period).
Day 85
|
2.0 units on the SGA scale
Standard Deviation 1.2
|
1.9 units on the SGA scale
Standard Deviation 1.2
|
1.8 units on the SGA scale
Standard Deviation 1.2
|
1.5 units on the SGA scale
Standard Deviation 1.2
|
OTHER_PRE_SPECIFIED outcome
Timeframe: Up to Cycle 5, Day 85.Population: The OL population was all randomised subjects who received any dose of OL Dysport®. Only subjects with data available for analysis at each time point are presented.
On each study visit per treatment cycle in the OL period, subjects were asked to assess the change, since the last treatment administration, in the appearance of their glabellar lines using the following 9-point Global Assessment Scale: +4 =100% improvement; +3 =75% improvement; +2 =50% improvement; +1 =25% improvement; 0 =no change; -1 =25% worsening; -2 =50%worsening; -3 =75% worsening; -4 =100% worsening. A responder, based on the SGA scale, was defined as having a grade of at least +2 (50% improvement). The proportion (percentage) of responders at each study visit on Day 8 to Day 85 in the OL period is presented.
Outcome measures
| Measure |
Dysport® 50 U - DB Period
n=424 Participants
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=355 Participants
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
n=232 Participants
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
n=98 Participants
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
|---|---|---|---|---|
|
The Proportion of Responders With Respect to the SGA Score at All Other Study Visits (OL Period).
Day 8
|
81.4 percentage of responders
Interval 77.3 to 85.0
|
75.5 percentage of responders
Interval 70.7 to 79.9
|
76.3 percentage of responders
Interval 70.3 to 81.6
|
62.2 percentage of responders
Interval 51.9 to 71.8
|
|
The Proportion of Responders With Respect to the SGA Score at All Other Study Visits (OL Period).
Day 29
|
82.1 percentage of responders
Interval 78.1 to 85.6
|
80.3 percentage of responders
Interval 75.8 to 84.3
|
75.4 percentage of responders
Interval 69.4 to 80.8
|
65.3 percentage of responders
Interval 55.0 to 74.6
|
|
The Proportion of Responders With Respect to the SGA Score at All Other Study Visits (OL Period).
Day 57
|
77.4 percentage of responders
Interval 73.1 to 81.3
|
74.4 percentage of responders
Interval 69.5 to 78.8
|
70.3 percentage of responders
Interval 63.9 to 76.1
|
66.3 percentage of responders
Interval 56.1 to 75.6
|
|
The Proportion of Responders With Respect to the SGA Score at All Other Study Visits (OL Period).
Day 85
|
63.4 percentage of responders
Interval 58.7 to 68.0
|
65.4 percentage of responders
Interval 60.1 to 70.3
|
61.6 percentage of responders
Interval 55.0 to 67.9
|
52.0 percentage of responders
Interval 41.7 to 62.2
|
OTHER_PRE_SPECIFIED outcome
Timeframe: Up to Cycle 5, Day 29.Population: The OL population was all randomised subjects who received any dose of OL Dysport®. Only subjects with data available for analysis is presented.
At cycle baseline (Day 1 of each treatment cycle) and Day 29 of each cycle in the OL period, subjects were asked to evaluate their age over the past 7 days at the time of assessment, using the following categories: * I look like my current age; * I look \_ years younger; * I look \_ years older. The mean change from cycle baseline in subject's self-perception of age at Day 29 of each cycle of the OL Period was calculated. A negative mean change from baseline in the subject's self-perception of age indicates that the subject's self-perception was to look younger compared with baseline.
Outcome measures
| Measure |
Dysport® 50 U - DB Period
n=410 Participants
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=347 Participants
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
n=225 Participants
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox Placebo - DB Period
n=97 Participants
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
|---|---|---|---|---|
|
Mean Change From Baseline in Subject's Self-Perception of Age at All Study Visits (OL Period)
|
-1.9 years
Standard Deviation 3.0
|
-1.6 years
Standard Deviation 2.9
|
-1.6 years
Standard Deviation 3.0
|
-1.1 years
Standard Deviation 2.4
|
Adverse Events
Dysport® 50 U - DB Period
Dysport® Placebo - DB Period
Botox 20 U - DB Period
Botox Placebo - DB Period
Dysport® 50 U - OL Period
Serious adverse events
| Measure |
Dysport® 50 U - DB Period
n=326 participants at risk
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=66 participants at risk
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
n=107 participants at risk
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1
|
Botox Placebo - DB Period
n=21 participants at risk
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® 50 U - OL Period
n=465 participants at risk
After the first treatment cycle, all eligible subjects entered the OL period and received Dysport® 50 U (0.25 mL), injected into five predefined sites across the glabellar region. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites per treatment cycle.
Subjects received a maximum of four treatment cycles (Cycles 2 to 5) with Dysport®. These cycles occurred at intervals of no less than 84 days (12 weeks) between each cycle, depending upon individual duration of response to Dysport® treatment. Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study
|
|---|---|---|---|---|---|
|
Eye disorders
Cataract
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.93%
1/107 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/465 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Gastrointestinal disorders
Large intestine polyp
|
0.31%
1/326 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/465 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Hepatobiliary disorders
Hyperplastic cholecystopathy
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.93%
1/107 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/465 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Infections and infestations
Appendicitis
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
1.5%
1/66 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/465 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Infections and infestations
Chronic tonsillitis
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
1.5%
1/66 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/465 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Infections and infestations
Herpes zoster
|
0.31%
1/326 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/465 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Injury, poisoning and procedural complications
Ankle fracture
|
0.31%
1/326 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/465 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Injury, poisoning and procedural complications
Contusion
|
0.31%
1/326 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/465 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Injury, poisoning and procedural complications
Spinal compression fracture
|
0.31%
1/326 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/465 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Musculoskeletal and connective tissue disorders
Spinal osteoarthritis
|
0.31%
1/326 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/465 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Papillary thyroid cancer
|
0.31%
1/326 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/465 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Skin and subcutaneous tissue disorders
Eczema
|
0.31%
1/326 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Endocrine disorders
Goitre
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Gastrointestinal disorders
Intestinal obstruction
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Hepatobiliary disorders
Cholelithiasis
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.43%
2/465 • Number of events 2 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Infections and infestations
Bronchitis
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Infections and infestations
Chronic sinusitis
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Infections and infestations
Pneumonia bacterial
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Infections and infestations
Urinary tract infection
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Injury, poisoning and procedural complications
Ligament injury
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Injury, poisoning and procedural complications
Ligament rupture
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 2 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Injury, poisoning and procedural complications
Radius fracture
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Musculoskeletal and connective tissue disorders
Intervertebral disc disorder
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Musculoskeletal and connective tissue disorders
Osteoarthritis
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Breast neoplasm
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Cervix carcinoma
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Colon cancer
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Endometrial cancer
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Fibroadenoma of breast
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Invasive breast carcinoma
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Rectal cancer
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Squamous cell carcinoma of the cervix
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Uterine leiomyoma
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.43%
2/465 • Number of events 2 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Nervous system disorders
Post herpetic neuralgia
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Pregnancy, puerperium and perinatal conditions
Ectopic pregnancy
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Reproductive system and breast disorders
Cervical polyp
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Reproductive system and breast disorders
Hydrosalpinx
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Reproductive system and breast disorders
Uterine haemorrhage
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Reproductive system and breast disorders
Uterine polyp
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Respiratory, thoracic and mediastinal disorders
Nasal septum deviation
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Surgical and medical procedures
Abortion induced
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Vascular disorders
Lymphocele
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
Other adverse events
| Measure |
Dysport® 50 U - DB Period
n=326 participants at risk
Subjects randomised to the Dysport® treatment group in Cycle 1 received on Day 1, 50 U (0.25 mL), divided into five injections into the glabellar area. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® Placebo - DB Period
n=66 participants at risk
Subjects randomised to the Dysport® placebo group in Cycle 1 received on Day 1, 0.25 mL, divided into five injections into the glabellar area. 0.05 mL of Dysport® placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Botox 20 U - DB Period
n=107 participants at risk
Subjects randomised to the Botox treatment group in Cycle 1 received on Day 1, 20 U (0.5 mL), divided into five injections into the glabellar area. 4 U (0.1 mL) of Botox was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1
|
Botox Placebo - DB Period
n=21 participants at risk
Subjects randomised to the Botox placebo group in Cycle 1 received on Day 1, 0. 5 mL, divided into five injections into the glabellar area. 0.1 mL of Botox placebo was administered intramuscularly, at right angles to the skin into each of the five injection sites. The Investigator was blinded with respect to treatment injection.
Following treatment administration, all subjects attended follow-up visits on Days 8, 29, 57 and 85 of Cycle 1. On Day 85, subjects were assessed for their eligibility to enter the OL period (Cycles 2 to 5). Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study. A subject was considered to have completed the study in Cycle 1 if they were not eligible for retreatment and had completed a total of 15 months follow-up following study treatment administration on Day 1.
|
Dysport® 50 U - OL Period
n=465 participants at risk
After the first treatment cycle, all eligible subjects entered the OL period and received Dysport® 50 U (0.25 mL), injected into five predefined sites across the glabellar region. 10 U (0.05 mL) of Dysport® was administered intramuscularly, at right angles to the skin into each of the five injection sites per treatment cycle.
Subjects received a maximum of four treatment cycles (Cycles 2 to 5) with Dysport®. These cycles occurred at intervals of no less than 84 days (12 weeks) between each cycle, depending upon individual duration of response to Dysport® treatment. Any subjects not eligible for retreatment were evaluated every 28 days at additional follow-up visits until they were eligible for retreatment or had completed the study
|
|---|---|---|---|---|---|
|
Eye disorders
Eyelid oedema
|
2.1%
7/326 • Number of events 7 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.93%
1/107 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
1.3%
6/465 • Number of events 6 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Eye disorders
Eyelid ptosis
|
4.0%
13/326 • Number of events 13 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.93%
1/107 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
3.2%
15/465 • Number of events 16 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Gastrointestinal disorders
Abdominal pain upper
|
0.31%
1/326 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
3.0%
2/66 • Number of events 2 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.65%
3/465 • Number of events 4 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Infections and infestations
Upper respiratory tract infection
|
8.9%
29/326 • Number of events 35 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
6.1%
4/66 • Number of events 5 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
11.2%
12/107 • Number of events 13 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
15.9%
74/465 • Number of events 94 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Infections and infestations
Viral upper respiratory tract infection
|
4.6%
15/326 • Number of events 18 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
4.5%
3/66 • Number of events 3 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
3.7%
4/107 • Number of events 4 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
5.4%
25/465 • Number of events 27 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Musculoskeletal and connective tissue disorders
Arthritis
|
0.61%
2/326 • Number of events 2 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.93%
1/107 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
4.8%
1/21 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.22%
1/465 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Nervous system disorders
Headache
|
2.8%
9/326 • Number of events 10 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.93%
1/107 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
1.9%
9/465 • Number of events 10 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Respiratory, thoracic and mediastinal disorders
Oropharyngeal pain
|
0.61%
2/326 • Number of events 2 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
1.5%
1/66 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
4.8%
1/21 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
1.3%
6/465 • Number of events 6 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Skin and subcutaneous tissue disorders
Dermatitis
|
0.92%
3/326 • Number of events 4 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
2.8%
3/107 • Number of events 3 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.43%
2/465 • Number of events 2 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Skin and subcutaneous tissue disorders
Dermatitis allergic
|
0.31%
1/326 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
4.8%
1/21 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.65%
3/465 • Number of events 3 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Skin and subcutaneous tissue disorders
Neurodermatitis
|
0.00%
0/326 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
4.8%
1/21 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/465 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Gastrointestinal disorders
Dental caries
|
1.2%
4/326 • Number of events 4 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/107 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
2.2%
10/465 • Number of events 10 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Metabolism and nutrition disorders
Hyperlipidaemia
|
1.5%
5/326 • Number of events 5 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.93%
1/107 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
2.6%
12/465 • Number of events 13 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
|
Respiratory, thoracic and mediastinal disorders
Cough
|
1.2%
4/326 • Number of events 4 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/66 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.93%
1/107 • Number of events 1 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
0.00%
0/21 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
2.6%
12/465 • Number of events 14 • Treatment emergent adverse events (TEAEs) were defined as any adverse event with start date on or after the first injection of study treatment or with start date prior to the first injection of study treatment but the intensity increased after the first injection of study treatment. TEAEs were collected until the end of Cycle 5 of the OL period, over a total timeframe of up to approximately 29 months.
The safety population consisted of all randomised subjects who received at least one injection of study treatment into at least one injection site. The safety population was analysed based on the treatment the subject actually received rather than the treatment to which the subject was randomised. The 1 subject who was randomised to Botox placebo group but received treatment of Dysport® 50 U in Cycle 1 was included in the Dysport® 50 U group and excluded from the Botox placebo group.
|
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee The disclosure restriction on the PI is that the sponsor must review all results communications prior to public release. The sponsor has the right to delay a publication by 60 days from the time submitted to the sponsor for review. Any factual amendments proposed by sponsor will be incorporated, provided that they do not alter the scientific value of the material.
- Publication restrictions are in place
Restriction type: OTHER