drugset / Trial / NCT00831415

Study Evaluating Long-Term Safety of Desvenlafaxine Succinate Sustained Release With Japanese Adult Subjects in Major Depressive Disorder (MDD)

NCT00831415

Phase 3 Completed 304 enrolled Pfizer
NaSingle-groupOpen-labelTreatment

Summary

The primary objective of this study is to evaluate the long-term safety of desvenlafaxine succinate sustained release tablets during 10-month open-label treatment of Japanese subjects with major depressive disorder (MDD). The secondary objective is to evaluate the long-term response of subjects receiving desvenlafaxine succinate sustained release tablets by clinical global evaluation, general well-being and absence of symptoms.

Timeline

Start
2009-03
Primary completion
2011-03
Completion
2011-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Desvenlafaxine Other / unclassified 25 mg Oral
Subject Desvenlafaxine Other / unclassified 50 mg Oral
Subject Desvenlafaxine Other / unclassified 100 mg Oral