drugset / Trial / NCT01371721
A 6-Month Open-Label Extension Study to the B2061014 Study to Evaluate the Safety, Tolerability and Efficacy of DVS SR in the Treatment of Children and Adolescents With MDD
Open-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
- Primary completion
- 2015-10
- Completion
- 2015-10
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 | — |