Overview

Safety and Efficacy of LibiGelĀ® for the Treatment of Hypoactive Sexual Desire Disorder in Surgically Menopausal Women

Status:
Completed
Trial end date:
2011-09-01
Target enrollment:
Participant gender:
Summary
This study is a randomized, double-blind, placebo-controlled, multi-center study of the safety and efficacy of LibiGelĀ® 300mcg in the treatment of HSDD in surgically menopausal women
Phase:
Phase 3
Details
Lead Sponsor:
BioSante Pharmaceuticals
Treatments:
Methyltestosterone
Testosterone
Testosterone 17 beta-cypionate
Testosterone enanthate
Testosterone undecanoate