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Last Updated: November 4, 2024

CLINICAL TRIALS PROFILE FOR FLIBANSERIN


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All Clinical Trials for flibanserin

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00277914 ↗ Flibanserin Randomized Withdrawal Trial in Pre-menopausal Women Completed Sprout Pharmaceuticals, Inc Phase 3 2006-01-01 To estimate the duration of efficacy with continued treatment of double-blind flibanserin or placebo over twenty-four weeks of treatment.
NCT00360243 ↗ 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.
NCT00360529 ↗ 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.
NCT00360555 ↗ 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.
NCT00441558 ↗ 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.
NCT00491829 ↗ Flibanserin Versus Placebo in Premenopausal Women With HSDD Completed Sprout Pharmaceuticals, Inc Phase 3 2007-06-01 To establish efficacy of Flibanserin 50 Milligrams Daily and 100 Milligrams Daily in 6-month treatment, vs placebo for Hypoactive Sexual Desire Disorder in premenopausal European women. To evaluate safety and tolerability of flibanserin in such patients.
NCT00601367 ↗ Flibanserin Evaluation Over 28 Additional Weeks in Hypoactive Sexual Desire Disorder Completed Sprout Pharmaceuticals, Inc Phase 3 2008-01-01 Safety profile of flibanserin over 28 additional weeks Distribution of preferred dose regimens
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for flibanserin

Condition Name

Condition Name for flibanserin
Intervention Trials
Sexual Dysfunctions, Psychological 13
Healthy 2
Hypoactive Sexual Desire Disorder 2
Depression 1
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Condition MeSH

Condition MeSH for flibanserin
Intervention Trials
Sexual Dysfunctions, Psychological 16
Hypokinesia 2
Adenocarcinoma 1
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Clinical Trial Locations for flibanserin

Trials by Country

Trials by Country for flibanserin
Location Trials
United States 311
Canada 44
Germany 3
Finland 2
Hungary 2
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Trials by US State

Trials by US State for flibanserin
Location Trials
Illinois 11
Florida 11
California 11
Texas 11
Tennessee 11
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Clinical Trial Progress for flibanserin

Clinical Trial Phase

Clinical Trial Phase for flibanserin
Clinical Trial Phase Trials
Phase 4 1
Phase 3 12
Phase 2 2
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Clinical Trial Status

Clinical Trial Status for flibanserin
Clinical Trial Phase Trials
Completed 11
Terminated 5
Recruiting 2
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Clinical Trial Sponsors for flibanserin

Sponsor Name

Sponsor Name for flibanserin
Sponsor Trials
Sprout Pharmaceuticals, Inc 14
Boehringer Ingelheim 1
San Diego Sexual Medicine 1
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Sponsor Type

Sponsor Type for flibanserin
Sponsor Trials
Industry 16
Other 5
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