drugset / Trial / NCT00252330

Efficacy and Safety of SR58611A in Patients With Major Depressive Disorder

NCT00252330

Phase 3 Completed 476 enrolled Sanofi
RandomizedParallel-groupDouble-blindTreatment

Summary

To evaluate the efficacy of a fixed dose of SR58611A(350 mg q12) compared to placebo in patients with MajorDepressive Disorder (MDD) using escitalopram (10 mgqd) as positive control. In addition, the tolerability and safety of SR58611A in patients with MDD will be evaluated.

Timeline

Start
2005-09
Primary completion
2007-01
Completion
2007-01

Drugs

EvaluationDrugModalityDoseRoute
Subject amibegron Small molecule 350 mg