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A Preliminary Clinical Study to Evaluate Fispemifene in the Treatment of Hypogonadism

Hypogonadism Clinical Trial

Official title:
Preliminary Efficacy and Safety of Fispemifene in the Treatment of Hypogonadism: A 4 Week, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study Comparing Daily Oral Doses of 100, 200, and 300 mg Fispemifene and Placebo

Clinical Trial Summary

The purpose of this study is to determine whether one or more fispemifene dose regimens are more effective than placebo in the treatment of hypogonadism in older men.

Clinical Trial Description

n/a

Study Design

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

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00290134
Study type Interventional
Source QuatRx Pharmaceuticals Company
Contact
Status Completed
Phase Phase 2
Start date February 2006
Completion date October 2007
View Details
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