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Last Updated: September 26, 2020

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CLINICAL TRIALS PROFILE FOR DESVENLAFAXINE

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All Clinical Trials for DESVENLAFAXINE

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00256685 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.
NCT00277823 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.
NCT00283842 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.
NCT00300378 Study Evaluating the Efficacy and Safety of Desvenlafaxine Tablets in Adult Outpatients With Major Depressive Disorder Completed Wyeth is now a wholly owned subsidiary of Pfizer Phase 3 2006-03-01 The primary objective is to compare the antidepressant efficacy, safety, and tolerability of DVS SR versus placebo in subjects with Major Depressive Disorder. Additional objectives include testing both general and functional quality-of-life outcomes and satisfaction with therapy reported by the subject.
NCT00329147 Study Evaluating the Effects of DVS SR and Paroxetine on the Pharmacokinetics of Desipramine in Healthy Subjects Completed Wyeth is now a wholly owned subsidiary of Pfizer Phase 3 2006-05-01 The purpose of this study is to evaluate the effects of multiple doses of DVS SR and paroxetine on the pharmacokinetics of a single dose of desipramine in healthy subjects.
NCT00329186 Study Evaluating the Pharmacokinetics of Venlafaxine ER and Desvenlafaxine SR in Healthy Subjects Completed Wyeth is now a wholly owned subsidiary of Pfizer Phase 3 2006-05-01 The purpose of this study is to determine if the relative difference in PK between extensive metabolizers (EMs) and poor metabolizers (PMs) is the same with desvenlafaxine SR and venlafaxine ER when a single dose is administered.
NCT00369343 Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) Versus Placebo in Peri- and Postmenopausal Women Completed Wyeth is now a wholly owned subsidiary of Pfizer Phase 3 2006-09-01 Desvenlafaxine succinate (DVS) is a potent and selective serotonin and norepinephrine reuptake inhibitor (SNRI). The sustained-release (SR) formulation, DVS SR, is being studied in the development program for the treatment of major depressive disorder (MDD), for vasomotor symptoms (VMS) associated with menopause, and for pain associated with peripheral diabetic neuropathy, as well as for the treatment of fibromyalgia syndrome. This study will investigate the safety, efficacy, and tolerability of DVS SR in women with MDD who are peri- and postmenopausal.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for DESVENLAFAXINE

Condition Name

Condition Name for DESVENLAFAXINE
Intervention Trials
Major Depressive Disorder 26
Depressive Disorder, Major 8
Depression 7
Vasomotor Symptoms 6
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Condition MeSH

Condition MeSH for DESVENLAFAXINE
Intervention Trials
Depression 44
Depressive Disorder 43
Depressive Disorder, Major 39
Disease 21
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Clinical Trial Locations for DESVENLAFAXINE

Trials by Country

Trials by Country for DESVENLAFAXINE
Location Trials
United States 476
Canada 28
Japan 21
South Africa 7
Mexico 6
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Trials by US State

Trials by US State for DESVENLAFAXINE
Location Trials
Florida 25
Ohio 22
California 21
Texas 19
Georgia 18
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Clinical Trial Progress for DESVENLAFAXINE

Clinical Trial Phase

Clinical Trial Phase for DESVENLAFAXINE
Clinical Trial Phase Trials
Phase 4 18
Phase 3 29
Phase 2/Phase 3 3
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Clinical Trial Status

Clinical Trial Status for DESVENLAFAXINE
Clinical Trial Phase Trials
Completed 45
Recruiting 7
Terminated 5
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Clinical Trial Sponsors for DESVENLAFAXINE

Sponsor Name

Sponsor Name for DESVENLAFAXINE
Sponsor Trials
Pfizer 26
Wyeth is now a wholly owned subsidiary of Pfizer 25
Luye Pharma Group Ltd. 3
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Sponsor Type

Sponsor Type for DESVENLAFAXINE
Sponsor Trials
Industry 57
Other 22
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