drugset / Trial / NCT00384033

Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) In The Treatment Of Major Depressive Disorder

NCT00384033 ↗

Phase 3 Completed 638 enrolled Pfizer
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary purpose of this study is to evaluate the efficacy and safety of two doses of DVS SR (50 and 100 mg/day) in the treatment of adults with Major Depressive Disorder.

Timeline

Start
2006-09
Primary completion
2007-09
Completion
2007-09

Outcome

Missed primary endpoint

paper The primary end point did not reach significance based on the global F test for controlling multiplicity of the desvenlafaxine doses. PMID 19698901 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Desvenlafaxine Other / unclassified 50 mg —
Subject Desvenlafaxine Other / unclassified 100 mg —
Subject Duloxetine Small molecule 60 mg —