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

Sexual Dysfunctions, Psychological Clinical Trial

Official title:
Open-label Extension Trial for Pre- and Postmenopausal Women With HSDD

Clinical Trial 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).

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

  • Sexual Dysfunctions, Psychological
Clinical Trial Details
NCT number NCT01103362
Study type Interventional
Source Sprout Pharmaceuticals, Inc
Contact
Status Terminated
Phase Phase 3
Start date April 2010
Completion date January 2011
View Details
See also
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