Clinical trial
An Eight-Week Study to Evaluate the Efficacy and Safety of Saredutant in…
NCT00250627 · Sanofi, Industry · Completed
Key facts
| NCT number | NCT00250627 |
|---|---|
| Title | An Eight-Week Study to Evaluate the Efficacy and Safety of Saredutant in Patients With Depression |
| Official title | An Eight-Week, Multicenter, Double-Blind, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Tolerability of One Fixed 100 mg Dose of Saredutant in Patients With Major Depressive Disorder |
| Lead sponsor | Sanofi, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Depressive Disorder |
| Intervention type | Drug |
| Interventions | Saredutant succinate (SR48968C) |
| Enrollment | 465 |
| Start date | Dec 1, 2004 |
| Primary completion | Dec 1, 2006 |
| Completion | Dec 1, 2006 |
| First posted | Nov 8, 2005 |
| Last update posted | Dec 23, 2008 |
| Countries | Canada, Chile, Croatia, Czechia, France, Germany, Mexico, Portugal |
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: