Clinical trial

24-week Placebo-controlled Trial of Flibanserin Once Daily in Premenopausal…

NCT00360529 · Sprout Pharmaceuticals, Inc, Industry · Completed

Key facts

NCT number NCT00360529
Title 24-week Placebo-controlled Trial of Flibanserin Once Daily in Premenopausal Women With Hypoactive Sexual Desire Disorder
Official title A Twenty Four Week, Randomized, Double-Blind, Placebo-Controlled, Safety and Efficacy Trial of Flibanserin 50mg Every Evening and Flibanserin 100mg Every Evening in Women With Hypoactive Sexual Desire Disorder in North America
Lead sponsor Sprout Pharmaceuticals, Inc, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Sexual Dysfunctions, Psychological
Intervention type Drug
Interventions flibanserin
Enrollment 880
Start date Jul 1, 2006
Primary completion Apr 1, 2008
Completion Apr 1, 2008
First posted Aug 4, 2006
Last update posted Jun 27, 2016
Countries Canada, United States

At a glance

  • 10–99 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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