Sexual Arousal Disorder Clinical Trial
This 8 week at home study is designed to explore efficacy endpoints and evaluate the safety of intranasal Bremelanotide in women with Female Sexual Arousal Disorder. Efficacy will be assessed vs. a parallel placebo group.
n/a
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double-Blind
Status | Clinical Trial | Phase | |
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