drugset / Trial / NCT00092911

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

NCT00092911 ↗

Phase 3 Completed 244 enrolled Wyeth is now a wholly owned subsidiary of Pfizer
RandomizedParallel-groupDouble-blindTreatment

Summary

The main objective of this study is to compare the antidepressant efficacy and safety of DVS-233 SR versus placebo in adult outpatients with Major Depressive Disorder.

Timeline

Start
—
Primary completion
2005-05
Completion
2005-05

Drugs

EvaluationDrugModalityDoseRoute
Subject DVS-233 SR Unknown — —