A 6-Month Extension Study To The B2061032 Study To Evaluate The Safety, Tolerability, And Efficacy Of DVS SR In The Treatment Of Child And Adolescent Outpatients With MDD
PHASE3
This is a 6-month, open-label, flexible-dose study evaluating Desvenlafaxin...
Status
Completed
Location
The University Of Alabama At Birmingham, Office Of Psychiatric Research
Study Evaluating Desvenlafaxine Succinate Sustained-Release (DVS SR) In The Treatment Of Child And Adolescent Outpatients With Major Depressive Disorder
PHASE2
The primary purpose of this study is to test the safety and tolerability of...
Phase 1 Study To Test the Bioequivalence Between Two 25 mg Tablets vs. One 50 mg Tablet Under Fast/Fed Condition and Evaluate Food Effect of Desvenlafaxine Succinate Sustained Release (DVS SR)
PHASE1
To determine the bioequivalence of 2 tablets of 25 mg sustained release (SR...