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A Study of MK-6913 for the Treatment of Hot Flashes in Postmenopausal Women (6913-004)

Women Clinical Trial

Official title:
A Phase IIa, Randomized, Double-Blind, Placebo- and Active-Controlled Study to Examine MK-6913 for the Treatment of Vasomotor Symptoms in Postmenopausal Women

Clinical Trial Summary

This study will assess the safety, tolerability, and efficacy of MK-6913 for the treatment of moderate-to-very-severe vasomotor symptoms (hot flashes or hot flushes) in postmenopausal women. The primary study hypothesis is that one or more doses of MK-6913 will result in a significantly greater reduction from baseline, compared to placebo, in the number of moderate to very severe hot flashes after 4 weeks of treatment.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

  • Moderate to Severe Vasomotor Symptoms in Postmenopausal
  • Women
Clinical Trial Details
NCT number NCT01015677
Study type Interventional
Source Merck Sharp & Dohme Corp.
Contact
Status Terminated
Phase Phase 2
Start date December 17, 2009
Completion date July 30, 2010
View Details
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