drugset / Trial / NCT00046020

Study Evaluating Venlafaxine ER in Recurrent Depression

NCT00046020 ↗

Phase 4 Completed 1096 enrolled Wyeth is now a wholly owned subsidiary of Pfizer
Treatment

Summary

The purpose of this study is to review the long-term comparative efficacy of venlafaxine ER in achieving and sustaining remission (wellness) in patients with recurrent major depression

Timeline

Start
2000-08
Primary completion
2005-10
Completion
2005-10

Outcome

Met primary endpoint

paper 23.1% (95% CI = 15.3 to 30.9) for venlafaxine ER and 42.0% (95% CI = 31.8 to 52.2) for placebo (p = .005 PMID 17685736 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Venlafaxine Small molecule — —