drugset / Trial / NCT00252343

Efficacy and Safety of SR58611A in Patients With a Generalized Anxiety Disorder

NCT00252343

Phase 3 Completed 360 enrolled Sanofi
RandomizedParallel-groupDouble-blindTreatment

Summary

To evaluate the efficacy of a fixed dose of SR58611A (350mg q12) compared to placebo in patients with GeneralizedAnxiety Disorder (GAD) using escitalopram (10 mg qd) as positive control. To evaluate the tolerability and safety of SR58611A in patients with GAD.

Timeline

Start
2005-09
Primary completion
2007-02
Completion
2007-02

Drugs

EvaluationDrugModalityDoseRoute
Subject amibegron Small molecule 350 mg

Indications