Desvenlafaxine Succinate Sustained-Release (DVS SR)
Sponsors
Wyeth is now a wholly owned subsidiary of Pfizer, Pfizer
Conditions
DepressionDepressive DisorderDepressive Disorder, MajorDiabetic Neuropathy, PainfulHealthyMajor Depressive DisorderMenopauseVasomotor System
Phase 1
Phase 3
Study of the Safety and Efficacy of Desvenlafaxine Succinate for Vasomotor Symptoms in Postmenopausal Women
CompletedNCT00369434
Start: 2006-06-30End: 2007-02-28Target: 450Updated: 2007-06-01
Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) In The Treatment Of Major Depressive Disorder
CompletedNCT00384033
Start: 2006-09-30End: 2007-09-30Updated: 2012-03-15
Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) vs. Escitalopram in Postmenopausal Women
CompletedNCT00406640
Start: 2006-12-31End: 2008-10-31Updated: 2023-12-28
Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) in the Treatment of Major Depressive Disorder
CompletedNCT00798707
Start: 2008-12-31End: 2010-04-30Updated: 2011-06-10
Study Evaluating the Long-Term Safety of Desvenlafaxine Succinate Sustained-Release (DVS SR) in Subjects With Pain Associated With Diabetic Peripheral Neuropathy
TerminatedNCT01050218
Start: 2006-07-31End: 2009-01-31Updated: 2023-12-11