drugset / Trial / NCT01121484

Study Evaluating Desvenlafaxine Succinate Sustained-Release (DVS SR) In The Treatment Of Peri- And Postmenopausal Women With Major Depressive Disorder (DVS 3364)

NCT01121484

Phase 4 Completed 439 enrolled Pfizer
RandomizedParallel-groupQuadruple-blindTreatment

Summary

A multicenter, 10-week study to evaluate the efficacy and safety of 50 mg of desvenlafaxine succinate sustained-release formulation (DVS SR) versus placebo in the treatment of peri- and postmenopausal women with major depressive disorder

Timeline

Start
2010-06
Primary completion
2011-06
Completion
2011-06

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Desvenlafaxine Other / unclassified 50 mg Oral