drugset / Trial / NCT01371721

A 6-Month Open-Label Extension Study to the B2061014 Study to Evaluate the Safety, Tolerability and Efficacy of DVS SR in the Treatment of Children and Adolescents With MDD

NCT01371721

Phase 3 Completed 269 enrolled Pfizer
Open-labelTreatment

Summary

This is a 6-month, open-label, flexible-dose study evaluating desvenlafaxine succinate sustained release (DVS SR) in the treatment of child and adolescent outpatients with major depressive disorder (MDD).

Timeline

Start
2012-02
Primary completion
2015-10
Completion
2015-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Desvenlafaxine Other / unclassified 20 mg
Subject Desvenlafaxine Other / unclassified 25 mg
Subject Desvenlafaxine Other / unclassified 35 mg
Subject Desvenlafaxine Other / unclassified 50 mg