drugset / Trial / NCT01103362
A 28-week Safety Study of Flibanserin in Pre- and Postmenopausal Women With Hypoactive Sexual Desire Disorder
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | flibanserin | Small molecule | 100 mg | Oral |