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

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    Recruiting
Updated on 23 November 2020

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).

 

Description

Details
Condition Generalized Anxiety Disorder (GAD - Pediatric)
Clinical Study IdentifierTX229382
Last Modified on23 November 2020

Eligibility

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Inclusion Criteria

Subjects, male or female, must be between 7 and 17 years old, inclusive, at the time of consent/assent and at the Baseline Visit
Subject weighs at least 20 kg
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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