drugset / Trial / NCT00277823

Study Evaluating Desvenlafaxine Sustained-Release (DVS-SR) in Adult Outpatients With Major Depressive Disorder

NCT00277823 ↗

Phase 3 Completed 480 enrolled Wyeth is now a wholly owned subsidiary of Pfizer
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to compare the antidepressant efficacy, safety, and tolerability of DVS-SR in subjects receiving daily doses of 50 mg or 100 mg of DVS-SR versus subjects receiving placebo.

Timeline

Start
2006-02
Primary completion
—
Completion
2007-01

Outcome

Met primary endpoint

paper Desvenlafaxine 50 mg was associated with a significantly greater adjusted mean change from baseline on the HAM-D(17) (-11.5) compared with placebo (-9.5, p=0.018) PMID 18507895 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject DVS-SR Unknown 50 mg —
Subject DVS-SR Unknown 100 mg —