An Eight-Week,Dble-Blind,Placebo-Controlled, Multicenter Study With Paroxetine (20 mg q24) as Positive Control, Evaluating the Efficacy, Safety and Tolerability of a Fixed Dose of SR58611A (350 mg q12) in Outpatients With Generalized Anxiety Disorder.

Trial Profile

An Eight-Week,Dble-Blind,Placebo-Controlled, Multicenter Study With Paroxetine (20 mg q24) as Positive Control, Evaluating the Efficacy, Safety and Tolerability of a Fixed Dose of SR58611A (350 mg q12) in Outpatients With Generalized Anxiety Disorder.

Completed
Phase of Trial: Phase III

Latest Information Update: 21 Jul 2011

At a glance

  • Drugs Amibegron (Primary)
  • Indications Generalised anxiety disorder
  • Focus Registrational; Therapeutic Use
  • Acronyms AQUARIUS
  • Sponsors Sanofi
  • Most Recent Events

    • 07 Jul 2009 Additional location identified as reported by ClinicalTrials.gov.
    • 07 Jul 2009 Actual patient number (366) added as reported by ClinicalTrials.gov.
    • 07 Jul 2009 Actual initiation date changed from Jan 2006 to Dec 2005 as reported by ClinicalTrials.gov.
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