drugset / Trial / NCT00256685

Study Evaluating DVS-233 SR to Treat Vasomotor Systems Associated With Menopause

NCT00256685

Phase 3 Completed 568 enrolled Wyeth is now a wholly owned subsidiary of Pfizer
RandomizedSingle-groupDouble-blindTreatment

Summary

The purpose of this study is to assess the safety and efficacy of desvenlafaxine succinate (DVS) for treatment of moderate to severe vasomotor symptoms (VMS) that are associated with menopause, and also to assess the effects of DVS on sleep parameters and health outcomes indicators.

Timeline

Start
2004-09
Primary completion
Completion
2005-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Desvenlafaxine Other / unclassified

Indications