drugset / Trial / NCT01235754

Extension Study to Assess Persistence of Benefit of LibiGel for the Treatment of Hypoactive Sexual Desire Disorder (HSDD)

NCT01235754

Phase 3 Completed 626 enrolled BioSante Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The objective of this study is to evaluate the persistence of benefit of LibiGel (testosterone gel) 300 mcg/day compared to placebo gel in a 12 week post-treatment period of Hypoactive Sexual Desire Disorder (HSDD) in surgically menopausal women.

Timeline

Start
2010-10
Primary completion
2011-12
Completion
2012-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Testosterone Small molecule 300 ug Other