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NCT00358631 · ClinicalTrials.gov registry record · Phase 2
An Eight-Week Study Evaluating the Efficacy and Tolerability of Two Doses of SSR149415 in Outpatients With Major Depressive Disorder
A Phase 2 study of Depressive Disorder, sponsored by Sanofi.
- Completed
- Registry status
- Phase 2
- Development phase
- 319
- Enrollment target
- 1
- Study location
NCT00358631 is a Phase 2 study of Depressive Disorder that has completed, run by Sanofi. The registered enrollment target is 319 participants, roughly in line with the 325-participant average among 47 other Depressive Disorder trials with a reported enrollment target. The trial reports 1 study location across 1 state.
The verdict
NCT00358631, a Phase 2 study of Depressive Disorder, has completed, sponsored by Sanofi.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 319 participants
- Enrollment target
- 1
- Study location
Study Summary
The objective is to evaluate the efficacy and safety of two doses of SSR149415 (250 mg and 100 mg twice daily) compared to placebo and escitalopram 10 mg once daily in outpatients with major depressive disorder.
Conditions Studied
Interventions
- DRUG SSR149415
Study Locations (1)
New Jersey
- Sanofi-Aventis - Bridgewater
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 319 participants |
| Start Date | 2006-07 |
| Est. Completion | 2007-12 |
| Phase | Phase 2 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00358631
The ClinicalTrials.gov registry entry for NCT00358631 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 319 participants, a figure that helps gauge the scale of data the investigators plan to collect, roughly in line with the 325-participant average among 47 other Depressive Disorder trials with a reported enrollment target. The listed sponsor is Sanofi, which has 713 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Depressive Disorder appearing as the primary indexed condition, and to 1 intervention - of which SSR149415 is the first listed.
NCT00358631 reports 1 study location spanning 1 distinct geographic area - top geographies include New Jersey.
Frequently Asked Questions
What is clinical trial NCT00358631 about?
NCT00358631 is a clinical study titled "An Eight-Week Study Evaluating the Efficacy and Tolerability of Two Doses of SSR149415 in Outpatients With Major Depressive Disorder". The objective is to evaluate the efficacy and safety of two doses of SSR149415 (250 mg and 100 mg twice daily) compared to placebo and escitalopram 10 mg once daily in outpatients with major depressive disorder.
What is the current status of trial NCT00358631?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 319 participants. The study started on 2006-07. Estimated completion is 2007-12.
What conditions does trial NCT00358631 study?
This clinical trial studies the following conditions: Depressive Disorder.
What interventions are being tested in trial NCT00358631?
The interventions under investigation include: SSR149415 (DRUG).
Who is sponsoring clinical trial NCT00358631?
This trial is sponsored by Sanofi, which has 713 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00358631 being conducted?
This trial has 1 study location across New Jersey. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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