drugset / Trial / NCT00358631

An Eight-Week Study Evaluating the Efficacy and Tolerability of Two Doses of SSR149415 in Outpatients With Major Depressive Disorder

NCT00358631

Phase 2 Completed 319 enrolled Sanofi
RandomizedParallel-groupDouble-blindTreatment

Summary

The objective is to evaluate the efficacy and safety of two doses of SSR149415 (250 mg and 100 mg twice daily) compared to placebo and escitalopram 10 mg once daily in outpatients with major depressive disorder.

Timeline

Start
2006-07
Primary completion
2007-12
Completion
2007-12

Drugs

EvaluationDrugModalityDoseRoute
Subject NELIVAPTAN Small molecule 100 mg
Subject NELIVAPTAN Small molecule 250 mg

Indications