drugset / Trial / NCT01103362

A 28-week Safety Study of Flibanserin in Pre- and Postmenopausal Women With Hypoactive Sexual Desire Disorder

NCT01103362 ↗

Phase 3 Terminated 596 enrolled Sprout Pharmaceuticals, Inc
NaSingle-groupOpen-labelTreatment

Summary

To generate additional long-term safety and efficacy data on flibanserin in premenopausal women and establish long-term safety and tolerability of flibanserin in naturally postmenopausal women with Hypoactive Sexual Desire Disorder who have completed a prior clinical trial of flibanserin (Trial 511.130, 511.147, or 511.156).

Timeline

Start
2010-04
Primary completion
2011-01
Completion
2011-01

Outcome

Outcome not reported

Stopped: “administrative reasons”

Drugs

EvaluationDrugModalityDoseRoute
Subject flibanserin Small molecule 100 mg Oral