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The primary objective of the study is to compare, after 8 weeks, the efficacy of SR58611A vs. placebo in patients with Major Depressive Disorder who are on concomitant treatment with escitalopram. Th...
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Lead Sponsor
Sanofi
NCT07088380 · Major Depressive Disorder, Treatment Resistant Depression
NCT06843187 · Major Depressive Disorder(MDD), Insomnia Comorbid to Psychiatric Disorder
NCT06564818 · Major Depressive Disorder
NCT06110897 · Major Depressive Disorder
NCT04751331 · Major Depressive Disorder
Sanofi-Aventis Administrative Office
Diegem
Sanofi-Aventis Administrative Office
Tatari
Sanofi-Aventis Administrative Office
Helsinki
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