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Clinical Trial Summary

The primary purpose of this study is to evaluate the long-term safety and tolerability of Desvenlafaxine Succinate Sustained-Release (DVS SR) in child and adolescent outpatients with major depressive disorder. A secondary aim is to evaluate the efficacy of DVS SR in the treatment of child and adolescent outpatients with major depressive disorder in an exploratory manner.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00669110
Study type Interventional
Source Wyeth is now a wholly owned subsidiary of Pfizer
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Status Completed
Phase Phase 2
Start date May 2008
Completion date May 2010