Trial Outcomes & Findings for 2. Study to Evaluate the Efficacy/Safety of Bremelanotide in Premenopausal Women With Hypoactive Sexual Desire Disorder (NCT NCT02338960)

NCT ID: NCT02338960

Last Updated: 2021-01-28

Results Overview

As measured by change from baseline to end-of-study in the desire domain from the FSFI (Question Q1 and Q2), 28-day recall, co-primary endpoint - FSFI desire domain This score is on a scale ranging from 1.2 to 6. A higher score on this scale represent an increase in sexual desire and is a better outcome.

Recruitment status

COMPLETED

Study phase

PHASE3

Target enrollment

714 participants

Primary outcome timeframe

8 weeks baseline plus 24 weeks (Main Study), 52 Weeks (OLE)

Results posted on

2021-01-28

Participant Flow

Core ("Main") Study consisted of a 4-week no drug Screening period, followed by a 4-week single blind PBO period, first dose administered in-clinic. Following the end of single-blind period, which served as Baseline, eligible subjects were then randomized to a 24-week double-blind outpatient treatment period, first dose administered in-clinic.

Core Study: 703 participants enrolled, 89 run-in failures 614 participants were randomized. OLE Study (optional): Of the 392 completers of the Core study, 321 participants enrolled in optional OLE study. The OLE Study was not reported.

Participant milestones

Participant milestones
Measure
Placebo PBO/BMT
Core Study: Subjects will self-administer a fixed dose of placebo subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 24 weeks. Placebo OLE Study: Subjects will self-administer a fixed dose of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks. bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Brememlanotide BMT/BMT
Core and OLE Study: Subjects will self-administer a fixed dose of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 24 weeks. bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Core Study
STARTED
306
308
Core Study
Received Intervention
303
301
Core Study
COMPLETED
219
173
Core Study
NOT COMPLETED
87
135
Open Label Extension
STARTED
191
130
Open Label Extension
COMPLETED
77
51
Open Label Extension
NOT COMPLETED
114
79

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Bremelanotide (BMT/BMT)
n=303 Participants
Subjects will self-administer a fixed dose of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours (Main) followed by a 52-week open label extension study (OLE) BMT/BMT bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Placebo (PBO/BMT)
n=301 Participants
Subjects will self-administer a fixed dose of placebo (PBO) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours (Main) followed by a 52-week open label extension study (OLE) where participants receive only BMT, no placebo PBO/BMT Placebo: Placebo bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Total
n=604 Participants
Total of all reporting groups
Age, Continuous
Main
38.5 years
STANDARD_DEVIATION 7.19 • n=303 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
39.1 years
STANDARD_DEVIATION 6.96 • n=301 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
38.8 years
STANDARD_DEVIATION 7.08 • n=604 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Age, Continuous
OLE
39.8 years
STANDARD_DEVIATION 7.12 • n=130 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
39.4 years
STANDARD_DEVIATION 6.54 • n=191 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
39.6 years
STANDARD_DEVIATION 6.77 • n=321 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Sex: Female, Male
Main · Female
303 Participants
n=303 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
301 Participants
n=301 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
604 Participants
n=604 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Sex: Female, Male
Main · Male
0 Participants
n=303 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
0 Participants
n=301 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
0 Participants
n=604 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Sex: Female, Male
OLE · Female
130 Participants
n=130 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
191 Participants
n=191 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
321 Participants
n=321 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Sex: Female, Male
OLE · Male
0 Participants
n=130 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
0 Participants
n=191 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
0 Participants
n=321 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Ethnicity (NIH/OMB)
Main · Hispanic or Latino
21 Participants
n=303 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
21 Participants
n=301 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
42 Participants
n=604 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Ethnicity (NIH/OMB)
Main · Not Hispanic or Latino
282 Participants
n=303 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
280 Participants
n=301 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
562 Participants
n=604 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Ethnicity (NIH/OMB)
Main · Unknown or Not Reported
0 Participants
n=303 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
0 Participants
n=301 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
0 Participants
n=604 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Ethnicity (NIH/OMB)
OLE · Hispanic or Latino
6 Participants
n=130 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
9 Participants
n=191 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
15 Participants
n=321 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Ethnicity (NIH/OMB)
OLE · Not Hispanic or Latino
124 Participants
n=130 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
182 Participants
n=191 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
306 Participants
n=321 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Ethnicity (NIH/OMB)
OLE · Unknown or Not Reported
0 Participants
n=130 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
0 Participants
n=191 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
0 Participants
n=321 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Race (NIH/OMB)
Main · American Indian or Alaska Native
2 Participants
n=303 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
1 Participants
n=301 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
3 Participants
n=604 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Race (NIH/OMB)
Main · Asian
5 Participants
n=303 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
4 Participants
n=301 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
9 Participants
n=604 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Race (NIH/OMB)
Main · Native Hawaiian or Other Pacific Islander
0 Participants
n=303 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
0 Participants
n=301 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
0 Participants
n=604 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Race (NIH/OMB)
Main · Black or African American
29 Participants
n=303 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
29 Participants
n=301 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
58 Participants
n=604 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Race (NIH/OMB)
Main · White
263 Participants
n=303 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
262 Participants
n=301 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
525 Participants
n=604 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Race (NIH/OMB)
Main · More than one race
3 Participants
n=303 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
2 Participants
n=301 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
5 Participants
n=604 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Race (NIH/OMB)
Main · Unknown or Not Reported
1 Participants
n=303 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
3 Participants
n=301 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
4 Participants
n=604 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Race (NIH/OMB)
OLE · American Indian or Alaska Native
0 Participants
n=130 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
0 Participants
n=191 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
0 Participants
n=321 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Race (NIH/OMB)
OLE · Asian
1 Participants
n=130 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
2 Participants
n=191 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
3 Participants
n=321 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Race (NIH/OMB)
OLE · Native Hawaiian or Other Pacific Islander
0 Participants
n=130 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
0 Participants
n=191 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
0 Participants
n=321 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Race (NIH/OMB)
OLE · Black or African American
10 Participants
n=130 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
15 Participants
n=191 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
25 Participants
n=321 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Race (NIH/OMB)
OLE · White
117 Participants
n=130 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
171 Participants
n=191 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
288 Participants
n=321 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Race (NIH/OMB)
OLE · More than one race
2 Participants
n=130 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
2 Participants
n=191 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
4 Participants
n=321 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
Race (NIH/OMB)
OLE · Unknown or Not Reported
0 Participants
n=130 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
1 Participants
n=191 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).
1 Participants
n=321 Participants • A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into OLE Study Phase, including 130 in the BMT group (BMT/BMT) and 191 in the PBO group (PBO/BMT).

PRIMARY outcome

Timeframe: 8 weeks baseline plus 24 weeks (Main Study), 52 Weeks (OLE)

Population: A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into the optional OLE Study Phase.

As measured by change from baseline to end-of-study in the desire domain from the FSFI (Question Q1 and Q2), 28-day recall, co-primary endpoint - FSFI desire domain This score is on a scale ranging from 1.2 to 6. A higher score on this scale represent an increase in sexual desire and is a better outcome.

Outcome measures

Outcome measures
Measure
Bremelanotide BMT/BMT
n=282 Participants
(Main Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 24 weeks (OLE Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Placebo PBO/BMT
n=288 Participants
(Main Study) PBO administered SC on an as-desired basis for 24 weeks Placebo: Placebo (OLE Study) subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Efficacy of a Fixed Dose of Bremelanotide as Measured by FSFI (Question Q1 and Q2), 28-day Recall.
Main study
0.63 score on a scale
Standard Deviation 1.036
0.21 score on a scale
Standard Deviation 0.922
Efficacy of a Fixed Dose of Bremelanotide as Measured by FSFI (Question Q1 and Q2), 28-day Recall.
Open label extension
1.25 score on a scale
Standard Deviation 1.158
0.70 score on a scale
Standard Deviation 1.220

PRIMARY outcome

Timeframe: 8 weeks baseline plus 24 weeks (Main Study), 52 Weeks (OLE)

Population: A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into the optional OLE Study Phase.

As measured by the change from baseline to End-of-Study of the Core Study in the bothered by low desire item from the FSDS-DAO (item 13). Responses range from 0 (never) to 4 (always). Lower scores on this scale represent an increase in sexual desire and indicate a better outcome. Higher scores indicate a worse outcome.

Outcome measures

Outcome measures
Measure
Bremelanotide BMT/BMT
n=282 Participants
(Main Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 24 weeks (OLE Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Placebo PBO/BMT
n=288 Participants
(Main Study) PBO administered SC on an as-desired basis for 24 weeks Placebo: Placebo (OLE Study) subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Efficacy of a Fixed Dose of Bremelanotide as Measured by FSDS-DAO (Item 13)
Main study
-0.71 score on a scale
Standard Deviation 1.145
-0.42 score on a scale
Standard Deviation 1.047
Efficacy of a Fixed Dose of Bremelanotide as Measured by FSDS-DAO (Item 13)
Open label extension
-1.4 score on a scale
Standard Deviation 1.20
-0.9 score on a scale
Standard Deviation 1.07

SECONDARY outcome

Timeframe: 8 weeks baseline plus 24 weeks (Main Study), 52 Weeks (OLE)

Population: A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into the optional OLE Study Phase. 128 participants in the OLE study completed the 52 weeks.

Mean change from Baseline to end of study (EOS) in the number of satisfying sexual events (SSEs) that occurred within 16 hours of study drug dosing and reported within 72 hours. An increase in number indicates a better outcome.

Outcome measures

Outcome measures
Measure
Bremelanotide BMT/BMT
n=282 Participants
(Main Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 24 weeks (OLE Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Placebo PBO/BMT
n=290 Participants
(Main Study) PBO administered SC on an as-desired basis for 24 weeks Placebo: Placebo (OLE Study) subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study (EOS) in the Number of Satisfying Sexual Events (SSEs) Associated With Study Drug Administration
Main study
0.0 events
Standard Deviation 1.34
0.0 events
Standard Deviation 1.20
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study (EOS) in the Number of Satisfying Sexual Events (SSEs) Associated With Study Drug Administration
Open label extension
0.19 events
Standard Deviation 1.997
-0.31 events
Standard Deviation 1.296

SECONDARY outcome

Timeframe: 8 weeks baseline plus 24 weeks (Main Study), 52 Weeks (OLE)

Population: A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into the optional OLE Study Phase. 128 participants in the OLE study completed the 52 weeks.

FSEP-R=Female Sexual Encounter Profile - Revised Scores on this scale range from 0 (no desire) to 3 (high desire). Scale is derived from a questionnaire (mean desire score) where an increase in value indicates a better outcome.

Outcome measures

Outcome measures
Measure
Bremelanotide BMT/BMT
n=282 Participants
(Main Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 24 weeks (OLE Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Placebo PBO/BMT
n=290 Participants
(Main Study) PBO administered SC on an as-desired basis for 24 weeks Placebo: Placebo (OLE Study) subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study in Mean Desire Score (Q3) From the FSEP-R
Main study
0.04 score on a scale
Standard Deviation 1.065
0.01 score on a scale
Standard Deviation 0.928
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study in Mean Desire Score (Q3) From the FSEP-R
Open label extension
0.43 score on a scale
Standard Deviation 1.095
0.33 score on a scale
Standard Deviation 1.023

SECONDARY outcome

Timeframe: 8 weeks baseline plus 24 weeks (Main Study), 52 Weeks (OLE)

Population: A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into the optional OLE Study Phase. 128 participants in the OLE study completed the 52 weeks.

FSEP-R=Female Sexual Encounter Profile - Revised Scores range from 0 (no desire) to 3 (high desire). Scale is derived from a questionnaire (mean desire score) where a higher score indicates a better outcome.

Outcome measures

Outcome measures
Measure
Bremelanotide BMT/BMT
n=282 Participants
(Main Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 24 weeks (OLE Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Placebo PBO/BMT
n=290 Participants
(Main Study) PBO administered SC on an as-desired basis for 24 weeks Placebo: Placebo (OLE Study) subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study in Mean Satisfaction With Desire Score (Q4) From FSEP-R
Main study
0.27 score on a scale
Standard Deviation 1.077
0.11 score on a scale
Standard Deviation 0.977
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study in Mean Satisfaction With Desire Score (Q4) From FSEP-R
Open label extension
0.76 score on a scale
Standard Deviation 1.127
0.47 score on a scale
Standard Deviation 1.075

SECONDARY outcome

Timeframe: 8 weeks baseline plus 24 weeks (Main Study), 52 Weeks (OLE)

Population: A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into the optional OLE Study Phase. 128 participants in the OLE study completed the 52 weeks.

FSDS-DAO = Female Sexual Distress Scale - Desire/Arousal/Orgasm. The FSDS-DAO is a validated 15-item self-assessment of sexual feelings and problems. All responses are on a scale ranging from 0 ("never") to 4 ("always"). Total Scores range from 0 (never feel bothered) to 60 (always feel bothered). Decreased scores indicate improvement. A higher score on this scale indicates a worse outcome. The score is the mean change from Baseline observed at EOS (Baseline score - EOS score)

Outcome measures

Outcome measures
Measure
Bremelanotide BMT/BMT
n=282 Participants
(Main Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 24 weeks (OLE Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Placebo PBO/BMT
n=285 Participants
(Main Study) PBO administered SC on an as-desired basis for 24 weeks Placebo: Placebo (OLE Study) subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study in the FSDS-DAO Total Score
Main study
-9.7 score on a scale
Standard Deviation 13.79
-5.6 score on a scale
Standard Deviation 12.06
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study in the FSDS-DAO Total Score
Open label extension
-18.4 score on a scale
Standard Deviation 14.06
-11.1 score on a scale
Standard Deviation 14.37

SECONDARY outcome

Timeframe: 8 weeks baseline plus 24 weeks (Main Study), 52 Weeks (OLE)

Population: A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into the optional OLE Study Phase. 128 participants in the OLE study completed the 52 weeks.

Female Sexual Function Index (FSFI) The score is computed programmatically \] resulting in a score on a scale ranging from 1.2 to 6 (Note: OLE: Open-label extension. Scores range from 2 to 36. An improvement in total FSFI score is an increase from baseline. A higher score on this scale represents an increase in sexual desire and is a better outcome.

Outcome measures

Outcome measures
Measure
Bremelanotide BMT/BMT
n=282 Participants
(Main Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 24 weeks (OLE Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Placebo PBO/BMT
n=288 Participants
(Main Study) PBO administered SC on an as-desired basis for 24 weeks Placebo: Placebo (OLE Study) subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study in the FSFI Total Score
Main study
2.45 score on a scale
Standard Deviation 7.383
0.84 score on a scale
Standard Deviation 5.879
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study in the FSFI Total Score
Open label extension
5.15 score on a scale
Standard Deviation 7.301
3.14 score on a scale
Standard Deviation 7.281

SECONDARY outcome

Timeframe: 8 weeks baseline plus 24 weeks (Main Study), 52 Weeks (OLE)

Population: A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into the optional OLE Study Phase. 128 participants in the OLE study completed the 52 weeks.

FSEP-R=Female Sexual Encounter Profile - Revised Scores on this scale range from 0 (no desire) to 3 (high desire) Scale is derived from a questionnaire (mean desire score) where a higher score indicates a better outcome.

Outcome measures

Outcome measures
Measure
Bremelanotide BMT/BMT
n=282 Participants
(Main Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 24 weeks (OLE Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Placebo PBO/BMT
n=290 Participants
(Main Study) PBO administered SC on an as-desired basis for 24 weeks Placebo: Placebo (OLE Study) subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study in the Mean Level of Sexual Arousal (Q6) From the FSEP-R
Main study
0.04 score on a scale
Standard Deviation 1.068
-0.01 score on a scale
Standard Deviation 0.906
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study in the Mean Level of Sexual Arousal (Q6) From the FSEP-R
Open label extension
0.33 score on a scale
Standard Deviation 0.987
0.35 score on a scale
Standard Deviation 0.994

SECONDARY outcome

Timeframe: 8 weeks baseline plus 24 weeks (Main Study), 52 Weeks (OLE)

Population: A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into the optional OLE Study Phase. 128 participants in the OLE study completed the 52 weeks.

FSEP-R=Female Sexual Encounter Profile - Revised Scores range from 0 (no desire) to 3 (high desire) Scale is derived from a questionnaire (mean desire score) where a higher score indicates a better outcome.

Outcome measures

Outcome measures
Measure
Bremelanotide BMT/BMT
n=282 Participants
(Main Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 24 weeks (OLE Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Placebo PBO/BMT
n=290 Participants
(Main Study) PBO administered SC on an as-desired basis for 24 weeks Placebo: Placebo (OLE Study) subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study in the Mean Satisfaction With Sexual Arousal (Q7) From the FSEP-R
Main study
0.23 score on a scale
Standard Deviation 1.112
0.09 score on a scale
Standard Deviation 0.974
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study in the Mean Satisfaction With Sexual Arousal (Q7) From the FSEP-R
Open label extension
0.60 score on a scale
Standard Deviation 1.107
0.47 score on a scale
Standard Deviation 1.102

SECONDARY outcome

Timeframe: 8 weeks baseline plus 24 weeks (Main Study), 52 Weeks (OLE)

Population: A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into the optional OLE Study Phase. 128 participants in the OLE study completed the 52 weeks.

FSDS-DAO = Female Sexual Distress Scale - Desire/Arousal/Orgasm. The FSDS-DAO is a validated 15-item self-assessment of sexual feelings and problems. Scores on this scale range from 0 ("never") to 4 ("always"). Decreased scores indicate improvement. A higher score on this scale indicates a worse outcome.

Outcome measures

Outcome measures
Measure
Bremelanotide BMT/BMT
n=282 Participants
(Main Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 24 weeks (OLE Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Placebo PBO/BMT
n=285 Participants
(Main Study) PBO administered SC on an as-desired basis for 24 weeks Placebo: Placebo (OLE Study) subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study in the Scored Time Spent Being Concerned by Difficulty With Sexual Arousal (Q14) From the FSDS-DAO
Main study
-0.8 score on a scale
Standard Deviation 1.23
-0.4 score on a scale
Standard Deviation 1.11
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study in the Scored Time Spent Being Concerned by Difficulty With Sexual Arousal (Q14) From the FSDS-DAO
Open label extension
-1.3 score on a scale
Standard Deviation 1.11
-0.9 score on a scale
Standard Deviation 1.17

SECONDARY outcome

Timeframe: 8 weeks baseline plus 24 weeks (Main Study), 52 Weeks (OLE)

Population: A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into the optional OLE Study Phase. 128 participants in the OLE study completed the 52 weeks.

Female Sexual Function Index (FSFI) The score is computed programmatically using the algorithm described by Rosen, resulting in a score ranging from 1.2 to 6. Higher scores on this scale represent an increase in sexual desire and is a better outcome.

Outcome measures

Outcome measures
Measure
Bremelanotide BMT/BMT
n=282 Participants
(Main Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 24 weeks (OLE Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Placebo PBO/BMT
n=288 Participants
(Main Study) PBO administered SC on an as-desired basis for 24 weeks Placebo: Placebo (OLE Study) subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study in the Arousal Domain of the FSFI (Q3 to Q6)
Open label extension
1.19 score on a scale
Standard Deviation 1.560
0.83 score on a scale
Standard Deviation 1.563
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study in the Arousal Domain of the FSFI (Q3 to Q6)
Main study
0.52 score on a scale
Standard Deviation 1.535
0.18 score on a scale
Standard Deviation 1.254

SECONDARY outcome

Timeframe: 8 weeks baseline plus 24 weeks (Main Study), 52 Weeks (OLE)

Population: A total 321 of the 392 (81.9%) subjects who completed the Core Study Phase continued into the optional OLE Study Phase. 128 participants in the OLE study completed the 52 weeks.

Change from Baseline to EOS in the total number of satisfying sexual events SSEs. A higher number of events indicates a better outcome.

Outcome measures

Outcome measures
Measure
Bremelanotide BMT/BMT
n=282 Participants
(Main Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 24 weeks (OLE Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Placebo PBO/BMT
n=290 Participants
(Main Study) PBO administered SC on an as-desired basis for 24 weeks Placebo: Placebo (OLE Study) subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study in the Total Number of SSEs
Main study
0.0 events
Standard Deviation 1.34
-0.0 events
Standard Deviation 1.20
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study in the Total Number of SSEs
Open label extension
0.25 events
Standard Deviation 2.376
-0.35 events
Standard Deviation 1.655

SECONDARY outcome

Timeframe: 24 weeks (Main Study)

Population: Completed double-blind study of Main study. OLE study was not a double blind study.

FSFI = Female Sexual Function Index The score is on a scale ranging from 1.2 to 6. A higher score on this scale represents an increase in sexual desire and is a better outcome.

Outcome measures

Outcome measures
Measure
Bremelanotide BMT/BMT
n=173 Participants
(Main Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 24 weeks (OLE Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Placebo PBO/BMT
n=219 Participants
(Main Study) PBO administered SC on an as-desired basis for 24 weeks Placebo: Placebo (OLE Study) subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study in the Desire Domain of the FSFI (Q1 to Q2) Throughout the Entirety of the Double-blind Phase
0.78 score on a scale
Standard Deviation 1.052
0.16 score on a scale
Standard Deviation 0.909

SECONDARY outcome

Timeframe: 24 weeks (Main Study)

Population: Completed double-blind study of Main study. OLE study wan not a double blind study.

FSDS-DAO = Female Sexual Distress Scale - Desire/Arousal/Orgasm. The FSDS-DAO is a validated 15-item self-assessment of sexual feelings and problems. The score is on a scale ranging from 0 ("never") to 4 ("always"). Decreased scores indicate improvement. A higher score indicates a worse outcome.

Outcome measures

Outcome measures
Measure
Bremelanotide BMT/BMT
n=173 Participants
(Main Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 24 weeks (OLE Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Placebo PBO/BMT
n=218 Participants
(Main Study) PBO administered SC on an as-desired basis for 24 weeks Placebo: Placebo (OLE Study) subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study in the Score for Feeling Bothered by Low Sexual Desire as Measured by the FSDS-DAO (Item 13) Throughout the Entirety of the Double-blind Phase
-0.8 score on a scale
Standard Deviation 1.22
-0.4 score on a scale
Standard Deviation 1.02

SECONDARY outcome

Timeframe: 24 weeks (Main Study)

Population: Completed double-blind study of Main study. OLE study wan not a double blind study.

Mean change from Baseline to EOS in the number of satisfying sexual events SSEs associated with study drug administration throughout the entirety of the double-blind phase. A higher number of events indicates a better outcome.

Outcome measures

Outcome measures
Measure
Bremelanotide BMT/BMT
n=177 Participants
(Main Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 24 weeks (OLE Study) Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Placebo PBO/BMT
n=221 Participants
(Main Study) PBO administered SC on an as-desired basis for 24 weeks Placebo: Placebo (OLE Study) subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours for 52 weeks Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Efficacy of a Fixed Dose of Bremelanotide, as Measured by the Change in Baseline to End of Study in the Number of SSEs Associated With Study Drug Administration Throughout the Entirety of the Double-blind Phase
0.1 events
Standard Deviation 1.37
-0.1 events
Standard Deviation 1.28

Adverse Events

Bremelanotide (Main Study)

Serious events: 3 serious events
Other events: 224 other events
Deaths: 0 deaths

Placebo (Main Study)

Serious events: 2 serious events
Other events: 137 other events
Deaths: 0 deaths

Bremelanotide (OLE)

Serious events: 1 serious events
Other events: 93 other events
Deaths: 0 deaths

Placebo (OLE)

Serious events: 0 serious events
Other events: 142 other events
Deaths: 0 deaths

Serious adverse events

Serious adverse events
Measure
Bremelanotide (Main Study)
n=303 participants at risk
Subjects will self-administer a fixed dose of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours. Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Placebo (Main Study)
n=301 participants at risk
Subjects will self-administer a fixed dose of placebo subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours. Placebo: Placebo
Bremelanotide (OLE)
n=130 participants at risk
Subjects will self-administer a fixed dose of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours. Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Placebo (OLE)
n=191 participants at risk
Subjects will self-administer a fixed dose of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours. Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Gastrointestinal disorders
Abdominal Pain
0.33%
1/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Colon cancer
0.33%
1/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.33%
1/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Blood and lymphatic system disorders
Anemia
0.00%
0/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.33%
1/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Infections and infestations
Pneumonia
0.33%
1/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Pregnancy, puerperium and perinatal conditions
Pregnancy
0.00%
0/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.33%
1/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Hepatobiliary disorders
cholecystitis
0.00%
0/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.77%
1/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Gastrointestinal disorders
Gastrointestinal inflammation
0.33%
1/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Uterine leiomyoma
0.33%
1/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.

Other adverse events

Other adverse events
Measure
Bremelanotide (Main Study)
n=303 participants at risk
Subjects will self-administer a fixed dose of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours. Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Placebo (Main Study)
n=301 participants at risk
Subjects will self-administer a fixed dose of placebo subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours. Placebo: Placebo
Bremelanotide (OLE)
n=130 participants at risk
Subjects will self-administer a fixed dose of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours. Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Placebo (OLE)
n=191 participants at risk
Subjects will self-administer a fixed dose of bremelanotide (BMT) subcutaneously (SC) via auto-injector on an as needed basis with no more than 1 dose taken every 24 hours. Bremelanotide: A melanocortin agonist and synthetic peptide analog of the naturally occurring hormone alpha-MSH (melanocyte-stimulating hormone)
Gastrointestinal disorders
Nausea
36.6%
111/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
28.5%
37/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
44.0%
84/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Gastrointestinal disorders
Vomiting
4.3%
13/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.33%
1/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
2.3%
3/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
4.7%
9/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Infections and infestations
Sinusitis
4.6%
14/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
4.3%
13/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
3.1%
4/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
4.7%
9/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Infections and infestations
Upper respiratory tract infection
4.0%
12/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
4.3%
13/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
3.8%
5/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
3.7%
7/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Infections and infestations
Urinary tract infection
3.3%
10/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
3.0%
9/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
3.1%
4/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
5.8%
11/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Infections and infestations
Nasopharyngitis
3.0%
9/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
6.0%
18/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
3.1%
4/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
5.2%
10/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
General disorders
Injection site pain
6.9%
21/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
5.6%
17/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
1.5%
2/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
2.6%
5/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
General disorders
Injection site reaction
5.3%
16/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
3.1%
4/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
2.6%
5/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
General disorders
Injection site erythema
3.3%
10/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
1.5%
2/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
1.6%
3/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
General disorders
Fatigue
2.6%
8/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.66%
2/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
2.3%
3/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
2.6%
5/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
General disorders
Injection site hematoma
2.3%
7/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
1.3%
4/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
2.1%
4/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Nervous system disorders
Headache
12.5%
38/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
1.3%
4/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
6.9%
9/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
15.2%
29/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Nervous system disorders
Paresthesia
3.0%
9/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.77%
1/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
2.1%
4/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Vascular disorders
Flushing
14.2%
43/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
8.5%
11/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
21.5%
41/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Vascular disorders
Hot flush
3.6%
11/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
4.2%
8/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Injury, poisoning and procedural complications
Sunburn
5.3%
16/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
9.3%
28/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
16.9%
22/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
13.1%
25/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Musculoskeletal and connective tissue disorders
Myalgia
2.0%
6/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.33%
1/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.77%
1/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
3.1%
6/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Respiratory, thoracic and mediastinal disorders
Cough
4.3%
13/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
1.3%
4/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
2.3%
3/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
3.7%
7/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Gastrointestinal disorders
Abdominal pain
1.7%
5/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.33%
1/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.77%
1/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
2.6%
5/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Gastrointestinal disorders
Abdominal discomfort
0.33%
1/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.33%
1/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
3.1%
4/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.52%
1/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Infections and infestations
Bronchitis
1.7%
5/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
1.3%
4/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
3.1%
4/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
1.0%
2/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Infections and infestations
Fungal infection
1.3%
4/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
1.3%
4/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
1.5%
2/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
2.1%
4/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Infections and infestations
Vulvovaginal mycotic infection
1.7%
5/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
1.7%
5/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
3.1%
6/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Nervous system disorders
Dizziness
1.3%
4/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.66%
2/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
2.6%
5/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Nervous system disorders
Migraine
0.00%
0/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.66%
2/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
2.3%
3/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
1.0%
2/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
General disorders
Influenza like illness
0.66%
2/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
1.5%
2/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
1.6%
3/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Skin and subcutaneous tissue disorders
Dermatitis contact
0.33%
1/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.77%
1/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
2.1%
4/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Skin and subcutaneous tissue disorders
Erythema
0.66%
2/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
2.1%
4/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Investigations
Blood creatine phophokinase
1.3%
4/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
2.1%
4/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Psychiatric disorders
Insomnia
0.66%
2/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
1.00%
3/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
2.1%
4/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
Psychiatric disorders
Depression
0.00%
0/303 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.33%
1/301 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
2.3%
3/130 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.
0.00%
0/191 • 1 year
Reporting participants: all subjects who were randomized and used at least 1 dose of double-blind study drug.

Additional Information

Medical Information

AMAG Pharmaceuticals

Phone: 1-877-411-2510

Results disclosure agreements

  • Principal investigator is a sponsor employee If there is no multi-site publication within 18 months after the Study has been completed or terminated at all Study sites, and all data have been received by Sponsor, the Site, and SMO shall have the right to publish its results from the Study for non-commercial purposes, if submitted to Sponsor for review 60 days prior to submission of publication. Publication must remove all confidential information and may be delayed by up to 180 days to allow Sponsor to protect its interests.
  • Publication restrictions are in place

Restriction type: OTHER