drugset / Trial / NCT01371708

A 6-Month Extension Study To The B2061032 Study To Evaluate The Safety, Tolerability, And Efficacy Of DVS SR In The Treatment Of Child And Adolescent Outpatients With MDD

NCT01371708

Phase 3 Completed 283 enrolled Pfizer
NaSingle-groupOpen-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
2012-02-02
Primary completion
2016-04-22
Completion
2016-04-22

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