6-mo. Min Eff Dose of Flibanserin: 25 v 50 mg Bid v 50 mg hs v Pbo in Younger Women in NA
Completed
Sprout Pharmaceuticals, Inc
Phase 3
2006-07-01
This trial is designed to assess the safety and efficacy of flibanserin in the treatment of
premenopausal women with Hypoactive Sexual Desire Disorder (HSDD) that meet standard
diagnostic criteria. Efficacy for flibanserin will be assessed vs. a parallel placebo group.
24-week Placebo-controlled Trial of Flibanserin Once Daily in Premenopausal Women With Hypoactive Sexual Desire Disorder
Completed
Sprout Pharmaceuticals, Inc
Phase 3
2006-07-01
This trial is designed to assess the safety and efficacy of flibanserin in the treatment of
premenopausal women with Hypoactive Sexual Desire Disorder (HSDD) that meets standard
diagnostic criteria. Efficacy for flibanserin will be assessed vs. a parallel placebo group.
Uptitration Trial of Flibanserin Versus Placebo in Premenopausal Women With Hypoactive Sexual Desire Disorder
Completed
Sprout Pharmaceuticals, Inc
Phase 3
2006-07-01
This trial is designed to assess the safety and efficacy of flibanserin in the treatment of
premenopausal women with Hypoactive Sexual Desire Disorder (HSDD) that meets standard
diagnostic criteria.
Efficacy for flibanserin will be assessed vs. a parallel placebo group.
A One-year Safety Study of Flibanserin to Treat Pre-Menopausal Women With Hypoactive Sexual Desire Disorder (HSDD).
Terminated
Sprout Pharmaceuticals, Inc
Phase 3
2007-02-01
To determine if long-term treatment with Flibanserin is safe and to monitor the effectiveness
of Flibanserin in Women with HSDD that have already completed a previous study
(511.70/71/.74/.75/.105) with Flibanserin.
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