A Study for the Treatment of Mania Associated With Bipolar I Disorder in Children and Adolescents

Study Identifier
M03-647
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact
Study Complete

Results Available

Scientific Result Summary
Available Language(s): English

Study Details

Medical Condition
  • Bipolar Disorder
  • Study Drug
  • Divalproex Sodium (Depakote ER)
  • Phase
    Phase 3
    Sex
    Female & Male
    Age
    10 - 17 Years

    Protocol Summary

    The purpose of the study is to evaluate the long-term safety profile of the Investigational

    Medication Depakote ER in the treatment of Bipolar I Disorder, manic or mixed episode, in

    children and adolescents ages 10-17.

    Study Locations

    Location
    Status
    Location
    PCSD Feighner Research
    San Diego, California, United States, 92111
    Status
    Not applicable
    Location
    PCSD Feighner Research
    San Marcos, California, United States, 92078
    Status
    Not applicable
    Location
    Altamonte Springs, Florida, United States, 32701
    Status
    Not applicable
    Location
    Segal Institute for Clinical Research
    Ft. Lauderdale, Florida, United States, 33319
    Status
    Not applicable
    Location
    Sarkis Clinical Trials
    Gainesville, Florida, United States, 32607
    Status
    Not applicable
    Location
    Segal Institute for Clinical Research
    North Miami, Florida, United States, 33161
    Status
    Not applicable
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