drugset / Trial / NCT01371734

A Study Of DVS SR In Treatment Of Children And Adolescent Outpatients With MDD

NCT01371734

Phase 3 Completed 363 enrolled Pfizer
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a double-blind study evaluating Desvenlafaxine Succinate Sustained-Release (DVS SR) versus placebo in the Treatment of Children and Adolescent Outpatients with Major Depressive Disorder (MDD).

Timeline

Start
2011-08
Primary completion
2015-09
Completion
2015-09

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