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
| Status: | Active, not recruiting |
|---|---|
| Conditions: | Depression, Major Depression Disorder (MDD) |
| Therapuetic Areas: | Psychiatry / Psychology, Pulmonary / Respiratory Diseases |
| Healthy: | No |
| Age Range: | 7 - 17 |
| Updated: | 4/21/2016 |
| Start Date: | February 2012 |
| End Date: | April 2016 |
A 6-month, Open-label, Multi-center, Flexible Dose Extension Study To The B2061032 Study To Evaluate The Safety, Tolerability And Efficacy Of Desvenlafaxine Succinate Sustained Release (Dvs Sr) Tablets In The Treatment Of Children And Adolescent Outpatients With Major Depressive Disorder
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).
Sustained-Release (DVS SR) in the Treatment of Child and Adolescent Outpatients with Major
Depressive Disorder (MDD).
Inclusion Criteria:
- Completed study B2061032 and who in the investigator's opinion, would benefit from
long term treatment with DVS SR
- Willingness and ability to comply with scheduled visits, treatment plan, and
procedures
Exclusion Criteria:
- Requires precaution against suicide
- Not in generally healthy medical condition
- Poor compliance with study drug or study procedures during participation in study
B2061032
We found this trial at
38
sites
Cleveland, Ohio 44106
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5601 Corporate Way
West Palm Beach, Florida 33407
West Palm Beach, Florida 33407
561-238-3036
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Birmingham, Alabama 35294
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Buffalo, New York 14215
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Glen Oaks, New York 11004
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The Hartford Hospital Hartford Hospital is the major teaching hospital affiliated with the University of...
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Virginia Commonwealth University Since our founding as a medical school in 1838, Virginia Commonwealth University...
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