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Sponsored by: |
Sanofi-Aventis |
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Information provided by: | Sanofi-Aventis |
ClinicalTrials.gov Identifier: | NCT00358631 |
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.
Condition | Intervention | Phase |
---|---|---|
Depressive Disorder |
Drug: SSR149415 |
Phase II |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study |
Official Title: | An Eight-Week, Multicenter, Double-Blind, Placebo- and Escitalopram-Controlled Study Evaluating the Efficacy and Tolerability of Two Fixed Doses of SSR149415 (250 mg Bid and 100 mg Bid) in Outpatients With Major Depressive Disorder |
Estimated Enrollment: | 312 |
Study Start Date: | July 2006 |
Ages Eligible for Study: | 18 Years to 64 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
The investigator will evaluate whether there are other reasons why a patient may not participate
Responsible Party: | sanofi-aventis ( ICD Study Director ) |
Study ID Numbers: | DFI5878, SSR149415 |
Study First Received: | July 31, 2006 |
Last Updated: | September 25, 2008 |
ClinicalTrials.gov Identifier: | NCT00358631 |
Health Authority: | United States: Food and Drug Administration |
depression antidepressive agents controlled clinical trial |
Depression Mental Disorders Mood Disorders Depressive Disorder, Major |
Dexetimide Depressive Disorder Citalopram Behavioral Symptoms |
Pathologic Processes Disease |