Depakote ER Plus an Atypical Antipsychotic Vs. an Atypical Antipsychotic Alone in the Treatment of Schizophrenia

Study Identifier
M02-547
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
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Study Complete

Results Available

Scientific Result Summary
Available Language(s): English

Study Details

Medical Condition
  • Schizophrenia
  • Study Drug
  • Divalproex Sodium Extended-Release Tablets
  • Olanzapine
  • Risperidone
  • Phase
    Phase 2
    Sex
    Female & Male
    Age
    18 - 65 Years

    Protocol Summary

    The purpose of this study is to assess the 14-day and 12-week safety and efficacy of Depakote

    ER used in combination with either olanzapine or risperidone versus antipsychotic monotherapy

    with olanzapine or risperidone for the treatment of schizophrenia.

    Study Locations

    Location
    Status
    Location
    Birmingham, Alabama, United States
    Status
    Not applicable
    Location
    Tuscaloosa, Alabama, United States
    Status
    Not applicable
    Location
    Anaheim, California, United States
    Status
    Not applicable
    Location
    Cerritos, California, United States
    Status
    Not applicable
    Location
    Chula Vista, California, United States
    Status
    Not applicable
    Location
    Garden Grove, California, United States
    Status
    Not applicable
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