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NCT00252330 · ClinicalTrials.gov registry record · Phase 3
Efficacy and Safety of SR58611A in Patients With Major Depressive Disorder
A Phase 3 study of Major Depressive Disorder, sponsored by Sanofi.
- Completed
- Registry status
- Phase 3
- Development phase
- 476
- Enrollment target
- 2
- Study locations
NCT00252330: Completed Phase 3 study of Major Depressive Disorder, sponsored by Sanofi.
NCT00252330 is a Phase 3 study of Major Depressive Disorder that has completed, run by Sanofi. The registered enrollment target is 476 participants, above the 375-participant average among 282 other Major Depressive Disorder trials with a reported enrollment target (27% higher). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00252330, a Phase 3 study of Major Depressive Disorder, has completed, sponsored by Sanofi.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 476 participants
- Enrollment target
- 2
- Study locations
Study Summary
To evaluate the efficacy of a fixed dose of SR58611A(350 mg q12) compared to placebo in patients with MajorDepressive Disorder (MDD) using escitalopram (10 mgqd) as positive control. In addition, the tolerability and safety of SR58611A in patients with MDD will be evaluated.
Conditions Studied
Interventions
- DRUG SR58611A
Study Locations (2)
New Jersey
- Sanofi-Aventis Administrative Office - Bridgewater
Other
- Sanofi-Aventis Administrative Office - Laval
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 476 participants |
| Start Date | 2005-09 |
| Est. Completion | 2007-01 |
| Phase | Phase 3 |
What the finished NCT00252330 record still lists
NCT00252330 is an interventional study that assigns participants to a tested intervention. The registered 476 participants enrollment target is mid-sized for trials with a published cap, above the 375-participant average among 282 other Major Depressive Disorder trials with a reported enrollment target (27% higher).
The record links to 1 condition, with Major Depressive Disorder appearing as the primary indexed condition, and to 1 intervention - of which SR58611A is the first listed.
NCT00252330 reports a single indexed study location in New Jersey, Other.
Frequently Asked Questions
What is clinical trial NCT00252330 about?
NCT00252330 is a clinical study titled "Efficacy and Safety of SR58611A in Patients With Major Depressive Disorder". To evaluate the efficacy of a fixed dose of SR58611A(350 mg q12) compared to placebo in patients with MajorDepressive Disorder (MDD) using escitalopram (10 mgqd) as positive control. In addition, the tolerability and safety of SR58611A in patients with MDD will be evaluated.
What is the current status of trial NCT00252330?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 476 participants. The study started on 2005-09. Estimated completion is 2007-01.
What conditions does trial NCT00252330 study?
This clinical trial studies the following conditions: Major Depressive Disorder.
What interventions are being tested in trial NCT00252330?
The interventions under investigation include: SR58611A (DRUG).
Who is sponsoring clinical trial NCT00252330?
This trial is sponsored by Sanofi, which has 713 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00252330 being conducted?
This trial has 2 study locations across New Jersey. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Major Depressive Disorder
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT00252330's enrollment target sits among peer trials
476 36th of 282 higher than 247 of 282 other Major Depressive Disorder trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Major Depressive Disorder trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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