drugset / Trial / NCT01309542
Long-Term Safety Of DVS-233 SR In Patients With Major Depressive Disorder
Non-randomizedSingle-groupOpen-labelTreatment
Summary
The study evaluated the long-term safety of Desvenlafaxine Succinate (DVS) Slow Release (SR) during open-label treatment in adult outpatients who had a primary diagnosis of major depressive disorder (MDD). The study also evaluated the long-term response of subjects receiving DVS SR for clinical global evaluation, functionality, general well-being, pain, and absence of depressive symptoms (remission).
Timeline
- Start
- 2003-08
- Primary completion
- 2006-03
- Completion
- 2006-03
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Desvenlafaxine | Other / unclassified | 200 mg | — |
| Subject | Desvenlafaxine | Other / unclassified | 400 mg | — |