Hypoactive Sexual Desire Disorder
Conditions
Keywords
KD-BMT-301, Bremelanotide
Brief summary
The purpose of this study is to Evaluate the Efficacy and Safety of Subcutaneously Administered Bremelanotide in Premenopausal Women with Hypoactive Sexual Desire Disorder(with or without Decreased Arousal).
Interventions
DRUGBremelanotide
Subjects will self-administer a fixed dose (1.75 mg) of bremelanotide (BMT) subcutaneously (SC) via auto-injector.
DRUGPlacebo
Subjects will self-administer a Placebo subcutaneously (SC) via auto-injector.
Sponsors
Kwang Dong Pharmaceutical co., ltd.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
FEMALE
Age
19 Years to No maximum
Healthy volunteers
No
Inclusion criteria
\[Main Inclusion Criteria\] * Has met diagnostic criteria for HSDD for at least 6 months * Is willing and able to understand and comply with all study requirements * Has a normal pelvic examination at screening \[Main
Exclusion criteria
\] * Subjects should be generally healthy premenopausal females with no psychological, gynecological or urological conditions which might contribute to the sexual dysfunction, compromise study participation, or confound interpretation of the study results * Not currently under treatment for the sexual dysfunction and willing to forego other treatments through the course of the clinical trial
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change from baseline to End of Study in the desire domain from the FSFI | Baseline up to End of Study(8weeks) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change from baseline to End of Study in FSDS-DAO (Item 13) | Baseline up to End of Study(8weeks) | — |
| Change from Baseline to End of Study in the Number of Satisfying Sexual Events (SSEs) Associated With Study Drug Administration | Baseline up to End of Study(8weeks) | — |
| Change from Baseline to End of Study in Mean Desire Score (Q3) From FSEP-R | Baseline up to End of Study(8weeks) | — |
| Change from Baseline to End of Study in Mean Satisfaction With Desire Score (Q4) From FSEP-R | Baseline up to End of Study(8weeks) | — |
| Change from Baseline to End of Study in the FSDS-DAO Total Score | Baseline up to End of Study(8weeks) | — |
| Change from Baseline to End of study in the total FSFI score based on the 19 questions | Baseline up to End of Study(8weeks) | The FSFI total score is on a scale ranging from 2 to 36. Increasing scores on this scale represent an increase in sexual desire and is a positive outcome. |
| Change from baseline in the desire domain from the FSFI Q1 and Q2 using all available double-blind data (visit 4, 5) | Baseline up to End of Study(8weeks) | — |
| Change in mean Level of Sexual Arousal from FSEP-R Q6 | Baseline up to End of Study(8weeks) | — |
| Change in mean Satisfaction with Sexual Arousal from FSEP-R Q7. | Baseline up to End of Study(8weeks) | — |
| Change from Baseline to End of study in the scored time spent being concerned by difficulty with sexual arousal as measured by the FSDS-DAO Q14. | Baseline up to End of Study(8weeks) | — |
| Change from Baseline to End of study in the arousal domain from the FSFI Q3 through Q6. | Baseline up to End of Study(8weeks) | — |
| Change from Baseline to End of study in the total number of SSEs. | Baseline up to End of Study(8weeks) | — |
| Change from baseline in the number of SSEs associated with study drug using the entire 8 weeks of the double-blind phase. | Baseline up to End of Study(8weeks) | — |
| Change from baseline in the score for feeling bothered by low sexual desire as measured by the FSDS -DAO Q13 using all available double-blind data(visit 4, 5) | Baseline up to End of Study(8weeks) | — |
Countries
South Korea
Outcome results
None listed