drugset / Trial / NCT00072774

Study Evaluating DVS-233 SR In Adult Outpatients With Major Depressive Disorder

NCT00072774

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

Summary

To compare the antidepressant efficacy and safety of subjects receiving DVS-233 SR versus subjects receiving placebo.

Timeline

Start
Primary completion
2004-11
Completion
2004-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Desvenlafaxine Other / unclassified 100 mg
Subject Desvenlafaxine Other / unclassified 200 mg
Subject Desvenlafaxine Other / unclassified 400 mg