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Efficacy and safety of Agomelatine (25 mg with potential adjustment at 50 mg) given orally once a day for 12 weeks in out-patients with Generalised Anxiety Disorder. A randomised flexible dose double-blind, placebo-controlled, parallel groups, international study.

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Study Phase

Phase 2

Therapeutic Area

Neuropsychiatric Diseases

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


Active Substance CodeS020098
Protocol CodeCL2-20098-040
EudraCT Code2004-002577-23

Documents and links

Results summary READ MORE
Scientific publication READ MORE

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