drugset / Trial / NCT00683592

Randomized, Double-Blind, Placebo Controlled Study of Vilazodone's Efficacy, Safety, and Biomarkers of Response in Major Depressive Disorder (MDD)

NCT00683592 ↗

Phase 3 Completed 481 enrolled Forest Laboratories
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This randomized, double-blind, placebo-controlled, multicenter, 8-week, clinical trial is designed to assess the efficacy and safety of vilazodone and to evaluate genetic biomarkers of treatment response associated with vilazodone use in adult patients diagnosed with MDD by the DSM-IV-TR criteria.

Timeline

Start
2008-03
Primary completion
2009-02
Completion
2009-03

Outcome

Met primary endpoint

registry p = 0.009; Difference in Least Squares Mean Change -2.5 (95% CI -4.4 to -0.6); ANCOVA NCT00683592 ↗

paper Vilazodone-treated patients had significantly greater improvement (P = .009) according to the MADRS than placebo patients (intent-to-treat; least-squares mean changes: -13.3, -10.8). PMID 21527122 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Vilazodone Small molecule 40 mg Oral