Clinical trial

An Eight-Week Study Evaluating the Efficacy of Two Fixed Doses (250 mg Twice…

NCT00361491 · Sanofi, Industry · Completed

Key facts

NCT number NCT00361491
Title An Eight-Week Study Evaluating the Efficacy of Two Fixed Doses (250 mg Twice Daily and 100 mg Twice Daily) of SSR149415 in Patients With Major Depressive Disorder
Official title An Eight-Week, Multicenter, Double-Blind, Placebo- and Paroxetine-Controlled Study Evaluating the Efficacy, and Tolerability of Two Fixed Doses of SSR149415 (250 mg Bid and 100 mg Bid) in Patients With Major Depressive Disorder
Acronym LENA
Lead sponsor Sanofi, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Depressive Disorder
Intervention type Drug
Interventions SSR149415
Enrollment 324
Start date Aug 1, 2006
Primary completion Sep 1, 2007
Completion Sep 1, 2007
First posted Aug 8, 2006
Last update posted Jan 16, 2009
Countries Argentina, Bulgaria, Canada, Chile, Croatia, Mexico, Russia

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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