drugset / Trial / NCT03463707

BP101 for Adults With Female Sexual Dysfunction

NCT03463707 ↗

Phase 3 Completed 205 enrolled Ivix LLX
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study is to confirm efficacy and safety of study drug BP101 in female patients with with decrease or loss of sexual desire, which is equal to acquired generalized hypoactive sexual desire disorder (HSDD). Patients will be randomized in 1:1 ratio to either BP101 or placebo arms.

Timeline

Start
2018-03-05
Primary completion
2018-11-26
Completion
2019-01-23

Drugs

EvaluationDrugModalityDoseRoute
Subject BP101 Unknown — Intranasal