Clinical trial
Efficacy, Safety and Tolerability of Agomelatine in the Treatment of Major…
NCT00411242 · Novartis, Industry · Completed
Key facts
| NCT number | NCT00411242 |
|---|---|
| Title | Efficacy, Safety and Tolerability of Agomelatine in the Treatment of Major Depressive Disorder |
| Official title | An 8-week, Randomized, Double-blind, Fixed Dosage, Placebo-controlled, Parallel-group, Multi-center Study of the Efficacy, Safety and Tolerability of Agomelatine 25 mg and 50 mg in the Treatment of Major Depressive Disorder (MDD) Followed by a 52-week, Open-label Extension (CAGO178A2302E) |
| Lead sponsor | Novartis, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Major Depressive Disorder (MDD) |
| Intervention type | Drug |
| Interventions | agomelatine, placebo |
| Enrollment | 503 |
| Start date | Dec 1, 2006 |
| Primary completion | Jan 1, 2008 |
| First posted | Dec 13, 2006 |
| Last update posted | Dec 23, 2020 |
| Countries | United States |
At a glance
- 10–99 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: