Expired Study
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Bridgewater, New Jersey 08807


Purpose:

The main purpose of this study is to evaluate the efficacy of saredutant 100mg or 30mg once daily in combination with paroxetine 20mg once daily compared to saredutant placebo in combination with paroxetine 20mg once daily in patients with major depressive disorder. The study also includes a double-placebo group (saredutant placebo in combination with paroxetine placebo).


Criteria:

Inclusion Criteria: - Outpatients with recurrent Major Depressive Disorder Exclusion Criteria: - Symptoms of current depressive episode for less than 30 days or more than 2 years - Mild depression, as measured by standard clinical research scales - Significant suicide risk - Lack of sexual activity (including masturbation) - Other psychiatric conditions that would obscure the results of the study - History of failure to respond to antidepressant treatment - Pregnancy or breast-feeding


NCT ID:

NCT00629551


Primary Contact:

Study Director
ICD CSD
Sanofi-Aventis


Backup Contact:

N/A


Location Contact:

Bridgewater, New Jersey 08807
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 19, 2018

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