A Randomized, Multicenter, Double-Blind, Flexibly-dosed, Efficacy and Safety Study of Escitalopram in the Treatment of Children and Adolescents With Generalized Anxiety Disorder

  • STATUS
    Not Recruiting
Updated on 11 August 2022

Summary

The primary objective of this study is to assess the safety and efficacy of escitalopram relative to placebo in the acute treatment of children (aged 7 through 11 years) and adolescents (aged 12 through 17 years) who meet criteria for generalized anxiety disorder (GAD) as defined in the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5).
 

Details
Condition Generalized Anxiety Disorder (GAD - Pediatric)
Clinical Study IdentifierTX229382
Last Modified on11 August 2022

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