Clinical trial
An Eight-Week Study to Evaluate the Efficacy and Safety of SR58611A in Patients…
NCT00266747 · Sanofi, Industry · Completed
Key facts
| NCT number | NCT00266747 |
|---|---|
| Title | An Eight-Week Study to Evaluate the Efficacy and Safety of SR58611A in Patients With Generalized Anxiety Disorder |
| Official title | 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 |
| Acronym | AQUARIUS |
| Lead sponsor | Sanofi, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Anxiety Disorders |
| Intervention type | Drug |
| Interventions | SR58611A |
| Enrollment | 366 |
| Start date | Dec 1, 2005 |
| Primary completion | Jan 1, 2007 |
| Completion | Jan 1, 2007 |
| First posted | Dec 19, 2005 |
| Last update posted | Mar 12, 2009 |
| Countries | Argentina, Austria, Estonia, France, Russia, South Africa, Sweden |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: