drugset / Trial / NCT03287232

Prasterone (DHEA) for the Treatment of Hypoactive Sexual Desire Disorder (HSDD)

NCT03287232

Phase 3 Completed 653 enrolled EndoCeutics Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective is to confirm the efficacy of intravaginal prasterone (DHEA) on Hypoactive Sexual Desire Disorder (HSDD) in postmenopausal women.

Timeline

Start
2017-10-16
Primary completion
2019-03-08
Completion
2019-07-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Dehydroepiandrosterone Other / unclassified 6.5 mg