Find Clinical Trial

Efficacy and safety of agomelatine (25mg/day with blinded potential adjustment to 50mg/day) versus escitalopram (10mg/day with blinded potential adjustment to 20mg/day) given orally for 12 weeks in non-depressed out-patients with severe Generalized Anxiety Disorder. A 12-week randomised, double-blind, versus escitalopram, 2-arm parallel groups, international multicenter study with a 9-month extension period


← Back
Study Phase

Phase 3

Therapeutic Area

Neuropsychiatric Diseases

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

AGOMELATINE,
S020098

Active Substance CodeS020098
Protocol CodeCL3-20098-089
EudraCT Code2012-003699-37


Documents and links

Results summary READ MORE
Scientific publication READ MORE




Quote

"Stein DJ; Khoo JP; Van Ameringen, D.M.; Hoschl C; Ahokas JT; Bauer M; Bitter I; Jarema M; Mosolov SN; Vavrusova L; Picarel Blanchot F; Matharan S; Olivier V Eur Neuropsychopharmacol. 2017; 27(Suppl. 4):S1003"




Servier Glossary of Terms

To ease the reading, we are developing a glossary of terms. In this glossary, we provide the lay terms used in our lay summaries and the corresponding medical terms. You will find the Servier Glossary of Terms on this link.



© 2024 LES LABORATOIRES SERVIER, an incorporated company of Servier.
All Rights Reserved. Servier does not sell its products over the Internet.
Accessibility