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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

NCT number NCT01057901
Study type Interventional
Source Sprout Pharmaceuticals, Inc
Contact
Status Terminated
Phase Phase 3
Start date January 2010
Completion date January 2011

See also
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