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Long-term efficacy and safety of agomelatine in non-depressed out-patients with Generalized Anxiety Disorder.A 26-week randomised double-blind placebo-controlled parallel group study following an open-label period of 16 weeks with agomelatine (25mg/day with the possibility for blinded dose-adjustment to 50mg/day).

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Study Phase

Phase 3

Therapeutic Area

Neuropsychiatric Diseases

IndicationGeneralised Anxiety Disorder
SponsorInstitut de Recherches Internationales Servier (I.R.I.S)
Active substance/
Medical device


Active Substance CodeS020098
Protocol CodeCL3-20098-050
EudraCT Code2006-005674-47

Documents and links

Results summary READ MORE
Scientific publication READ MORE

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