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
Completed · Phase 3
Conditions studied: Major Depressive Disorder
In brief
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).
Key facts
- Study ID
- NCT01371708
- Run by
- Pfizer
- People needed
- 283
- Starts
- 2012-02-02
- Expected to finish
- 2016-04-22
- Last updated by the study team
- 2017-07-27
Who can join
Age: 7 and older, up to 17. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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
You may not qualify if…
- Requires precaution against suicide
- Not in generally healthy medical condition
- Poor compliance with study drug or study procedures during participation in study B2061032
Where it is running
- The University Of Alabama At Birmingham, Office Of Psychiatric Research — Birmingham, Alabama, United States
- Center for Advanced Improvement — Tucson, Arizona, United States
- Sun Valley Research Center — Imperial, California, United States
- MCB Clinical Research Centers — Colorado Springs, Colorado, United States
- Institute of Living/Hartford Hospital — Hartford, Connecticut, United States
- SJS Clinical Research, Inc. — Destin, Florida, United States
- Sarkis Clinical Trials — Gainesville, Florida, United States
- Clinical Neuroscience Solutions — Jacksonville, Florida, United States
- Medical Research Group of Central Florida — Orange City, Florida, United States
- Millenia Psychiatry & Research, Inc. — Orlando, Florida, United States
- Janus Center for Psychiatric Research — West Palm Beach, Florida, United States
- Northwest Behavioral Research Center — Marietta, Georgia, United States
- Capstone Clinical Research — Libertyville, Illinois, United States
- Baber Research Group — Naperville, Illinois, United States
- Clinco — Terre Haute, Indiana, United States
- Pharmasite Research, Inc — Baltimore, Maryland, United States
- Millennium Psychiatric Associates, LLC — Creve Coeur, Missouri, United States
- Premier Psychiatric Research Institute, LLC — Lincoln, Nebraska, United States
- Erie County Medical Center/State University of New York (SUNY) at Buffalo Affiliate — Buffalo, New York, United States
- The Zucker Hillside Hospital, North Shore-Long Island Jewish Health System — Glen Oaks, New York, United States
- Bioscience Research, LLC. — Mount Kisco, New York, United States
- Finger Lakes Clinical Research — Rochester, New York, United States
- Stony Brook University Medical Center, child and Adolescent Psychiatry — Stony Brook, New York, United States
- Neuro-Behavioral Clinical Research, Inc. — Canton, Ohio, United States
- Discovery and Wellness Center for Children/University Hospitals Case Medical Center — Cleveland, Ohio, United States
Full record on ClinicalTrials.gov
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