drugset / Trial / NCT01361308

Efficacy/Safety Study of Brisdelle™ (Formerly Known as Mesafem) in the Treatment of Vasomotor Symptoms (VMS)

NCT01361308

Phase 3 Completed 614 enrolled Noven Therapeutics
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to assess the safety \& efficacy of Brisdelle (paroxetine mesylate) Capsules 7.5 mg for treatment of vasomotor symptoms (VMS) associated with menopause.

Timeline

Start
2011-05
Primary completion
2011-12
Completion
2012-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Paroxetine Small molecule 7.5 mg

Indications

No indication recorded.