drugset / Trial / NCT00863798

Study Evaluating Desvenlafaxine Succinate Sustained Release In Adults With Major Depressive Disorder

NCT00863798

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary purpose of this study is to compare the antidepressant efficacy and safety of two doses of desvenlafaxine succinate sustained release (10 and 50 mg/day) in adults with Major Depressive Disorder. The study will also assess changes in sexual function and general and functional quality of life outcomes.

Timeline

Start
2009-04
Primary completion
2010-03
Completion
2010-03

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Desvenlafaxine Other / unclassified 10 mg
Subject Desvenlafaxine Other / unclassified 50 mg