Clinical trial

Efficacy, Safety and Tolerability of Agomelatine in the Prevention of Relapse of…

NCT00467402 · Novartis, Industry · Completed

Key facts

NCT number NCT00467402
Title Efficacy, Safety and Tolerability of Agomelatine in the Prevention of Relapse of Major Depressive Disorder
Official title A 52-week, Randomized, Double-blind, Placebo-controlled, Multi-center, Parallel-group Study of the Long-term Efficacy, Tolerability and Safety of Agomelatine 25 and 50 mg in the Prevention of Relapse of Major Depressive Disorder (MDD) Following Open-label Treatment of 16-24 Weeks
Lead sponsor Novartis, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Major Depressive Disorder
Intervention type Drug
Interventions agomelatine, placebo
Enrollment 644
Start date Apr 1, 2007
Primary completion Sep 1, 2009
First posted Apr 30, 2007
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:

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