Study Evaluating DVS-233 SR to Treat Vasomotor Systems Associated With Menopause
Completed
Wyeth is now a wholly owned subsidiary of Pfizer
Phase 3
2004-09-01
The purpose of this study is to assess the safety and efficacy of desvenlafaxine succinate
(DVS) for treatment of moderate to severe vasomotor symptoms (VMS) that are associated with
menopause, and also to assess the effects of DVS on sleep parameters and health outcomes
indicators.
Study Evaluating Desvenlafaxine Sustained-Release (DVS-SR) in Adult Outpatients With Major Depressive Disorder
Completed
Wyeth is now a wholly owned subsidiary of Pfizer
Phase 3
2006-02-01
The purpose of this study is to compare the antidepressant efficacy, safety, and tolerability
of DVS-SR in subjects receiving daily doses of 50 mg or 100 mg of DVS-SR versus subjects
receiving placebo.
Study Evaluating Desvenlafaxine Succinate Sustained-release (DVS SR) in Adult Outpatients With Pain Associated With Diabetic Peripheral Neuropathy
Terminated
Wyeth is now a wholly owned subsidiary of Pfizer
Phase 3
2006-03-01
The purpose of this study is to evaluate the safety and efficacy of DVS SR in the treatment
of neuropathic pain associated with diabetic peripheral neuropathy.
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