drugset / Trial / NCT00319709

An Eight-Week Study to Evaluate the Efficacy and Safety of SR58611A in Elderly Patients With Depression

NCT00319709

Phase 3 Completed 288 enrolled Sanofi
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of the study is to evaluate the efficacy and safety of SR58611A in elderly patients with depression.The primary objective is to evaluate the efficacy of a 700 mg dose of SR58611A compared to placebo in elderly patients with depression. The secondary objectives are to evaluate the safety of SR58611A and to evaluate the efficacy of SR58611A on disability and quality of life in elderly patients with depression.

Timeline

Start
2006-04
Primary completion
2007-04
Completion
2007-08

Drugs

EvaluationDrugModalityDoseRoute
Subject amibegron Small molecule 700 mg

Indications