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Early effect of agomelatine on general interest in outpatients with Major Depressive Disorder. A 12-week, randomized, double-blind, multicentre study with parallel groups: agomelatine (25mg/day given orally with blinded potential adjustment to 50mg/day) versus escitalopram (10mg/day given orally with blinded potential adjustment to 20mg/day).


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Study Phase

Phase 3

Therapeutic Area

Neuropsychiatric Diseases

Active substance/
Medical device

S020098, AGOMELATINE

SponsorInstitut de Recherches Internationales Servier (I.R.I.S)
Active Substance CodeS020098
Protocol CodeCL3-20098-083
EudraCT Code2010-023576-10
ISRCTN CodeISRCTN28327843


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Results summary READ MORE




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