Clinical trial
Efficacy and Safety of SR58611A in Patients With Major Depressive Disorder…
NCT00385307 · Sanofi, Industry · Completed
Key facts
| NCT number | NCT00385307 |
|---|---|
| Title | Efficacy and Safety of SR58611A in Patients With Major Depressive Disorder (SIRIUS) |
| Official title | An Eight-Week, Double-Blind, Placebo-Controlled, Multicenter Study With Paroxetine (10 mg qd) as Positive Control, Evaluating the Efficacy, Safety, Tolerability of Two Fixed Doses of SR58611A (175 mg q12/ 350 mg q12) in Outpatients With MDD |
| Lead sponsor | Sanofi, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Major Depressive Disorder |
| Intervention type | Drug |
| Interventions | amibegron (SR58611A) |
| Enrollment | 680 |
| Start date | Sep 1, 2006 |
| Primary completion | Nov 1, 2007 |
| Completion | Nov 1, 2007 |
| First posted | Oct 9, 2006 |
| Last update posted | Mar 25, 2009 |
| Countries | United States |
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: