drugset / Trial / NCT00238719

Study Evaluating Venlafaxine ER in Children and Adolescents With Social Anxiety Disorder

NCT00238719

Phase 3 Completed 293 enrolled Wyeth is now a wholly owned subsidiary of Pfizer
RandomizedParallel-groupDouble-blindTreatment

Summary

To determine the anxiolytic efficacy, safety, and tolerability of a flexible-dose of venlafaxine extended release (ER) administered for 16 weeks in the treatment of children and adolescent outpatients with social anxiety disorder (generalized) in a placebo-controlled study.

Timeline

Start
1999-12
Primary completion
Completion
2003-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Venlafaxine Small molecule

Indications