Depakote Monotherapy, Olanzapine Monotherapy, and Combination Therapy of Depakote Plus Olanzapine in Stable Subjects During the Maintenance Phase of Bipolar Illness

Study Identifier
M02-551
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
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Results Available

Scientific Result Summary
Available Language(s): English

Study Details

Medical Condition
  • Bipolar Disorder
  • Study Drug
  • Divalproex Sodium (Delayed-Release Tablets)
  • Divalproex Sodium (Extended-Release Tablets)
  • Olanzapine
  • Phase
    Phase 4
    Sex
    Female & Male
    Age
    18 - 65 Years

    Protocol Summary

    The purpose of this study is to assess the efficacy and safety of continued combination

    therapy using Depakote plus olanzapine, vs. Depakote monotherapy and olanzapine monotherapy

    in stable subjects during the maintenance phase of bipolar illness.

    Study Locations

    Location
    Status
    Location
    Behavioral and Medical Research, LLC
    Anaheim, California, United States, 92805
    Status
    Not applicable
    Location
    Synergy Clinical Research
    Chula Vista, California, United States, 91910
    Status
    Not applicable
    Location
    Clinical Trial Management
    Fort Meyers, Florida, United States, 33907
    Status
    Not applicable
    Location
    Segal Institute for Clinical Research
    North Miami, Florida, United States, 33161
    Status
    Not applicable
    Location
    Rush Presbyterian - St. Luke's
    Chicago, Illinois, United States, 60612
    Status
    Not applicable
    Location
    University of Louisville Outpatient Psychiatry
    Louisville, Kentucky, United States, 40202
    Status
    Not applicable
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