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Flibanserin for the Treatment of Hypoactive Sexual Desire Disorder in Postmenopausal Women

Sexual Dysfunctions, Psychological Clinical Trial

Official title:
24-wk Efficacy and Safety of Flibanserin vs Pbo in Naturally Postmenopausal Women in United States

Clinical Trial Summary

The objective of this trial is to assess the safety and efficacy of 24-week course of flibanserin for the treatment of Hypoactive Sexual Desire Disorder (HSDD) in naturally postmenopausal women.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

  • Sexual Dysfunctions, Psychological
Clinical Trial Details
NCT number NCT00996372
Study type Interventional
Source Sprout Pharmaceuticals, Inc
Contact
Status Completed
Phase Phase 3
Start date October 2009
Completion date March 2011
View Details
See also
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