drugset / Trial / NCT01309542

Long-Term Safety Of DVS-233 SR In Patients With Major Depressive Disorder

NCT01309542

Phase 3 Completed 1403 enrolled Pfizer
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The study evaluated the long-term safety of Desvenlafaxine Succinate (DVS) Slow Release (SR) during open-label treatment in adult outpatients who had a primary diagnosis of major depressive disorder (MDD). The study also evaluated the long-term response of subjects receiving DVS SR for clinical global evaluation, functionality, general well-being, pain, and absence of depressive symptoms (remission).

Timeline

Start
2003-08
Primary completion
2006-03
Completion
2006-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Desvenlafaxine Other / unclassified 200 mg
Subject Desvenlafaxine Other / unclassified 400 mg