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A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Study To Evaluate The Efficacy, Safety And Tolerability Of Desvenlafaxine Succinate Sustained-release (Dvs Sr) In The Treatment Of Children And Adolescent Outpatients With Major Depressive Disorder
This is a double-blind study evaluating Desvenlafaxine Succinate Sustained-Release (DVS SR) versus placebo in the Treatment of Children and Adolescent Outpatients with Major Depressive Disorder (MDD).
Age
7 - 17 years
Sex
ALL
Healthy Volunteers
No
Children's Hospital of Alabama Laboratory
Birmingham, Alabama, United States
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
Bliss Basement Pharmacy - Hartford Hospital
Hartford, Connecticut, United States
Institute of Living/Hartford Hospital
Hartford, Connecticut, United States
Institute of Living
Hartford, Connecticut, United States
SJS Clinical Research, Inc.
Destin, Florida, United States
Sarkis Clinical Trials
Gainesville, Florida, United States
Start Date
August 1, 2011
Primary Completion Date
September 1, 2015
Completion Date
September 1, 2015
Last Updated
March 20, 2017
363
ACTUAL participants
Desvenlafaxine Succinate Sustained-Release
DRUG
Desvenlafaxine Succinate Sustained-Release
DRUG
Placebo
DRUG
Lead Sponsor
Pfizer
NCT07115329
NCT06793397
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07025720