drugset / Trial / NCT01371708
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
NaSingle-groupOpen-labelTreatment
Summary
This is a 6-month, open-label, flexible-dose study evaluating Desvenlafaxine Succinate Sustained-Release (DVS SR) in the Treatment of Child and Adolescent Outpatients with Major Depressive Disorder (MDD).
Timeline
- Start
- 2012-02-02
- Primary completion
- 2016-04-22
- Completion
- 2016-04-22
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Desvenlafaxine | Other / unclassified | 20 mg | — |
| Subject | Desvenlafaxine | Other / unclassified | 25 mg | — |
| Subject | Desvenlafaxine | Other / unclassified | 35 mg | — |
| Subject | Desvenlafaxine | Other / unclassified | 50 mg | — |