drugset / Trial / NCT00390533

An Eight-week Study to Evaluate the Efficacy and Safety of 2 Doses of Saredutant in Patients With Generalized Anxiety Disorder

NCT00390533

Phase 3 Completed 428 enrolled Sanofi
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective is to evaluate the efficacy of two fixed doses (100 mg and 30 mg once daily) of saredutant compared to placebo in patients with generalized anxiety disorder. The secondary objectives are to evaluate the efficacy of saredutant on disability and quality of life in patients with generalized anxiety disorder, and to evaluate blood levels of saredutant.

Timeline

Start
2006-09
Primary completion
2008-02
Completion
2008-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Saredutant Small molecule 30 mg Oral
Subject Saredutant Small molecule 100 mg Oral