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
For general inquiries, please contact
Study Complete
Results Available
Scientific Result Summary
Available Language(s): English
Study Details
Medical Condition
Study Drug
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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