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A Randomized, Double-Blind, Risperidone-Reference, Parallel-Group, Safety, and Tolerability Study of Vabicaserin (SCA-136) in Japanese Subjects With Acute Exacerbation of Schizophrenia
This study will evaluate the clinical safety and tolerability of vabicaserin in Japanese subjects that have a sudden worsening of their symptoms of schizophrenia. The study will also assess the efficacy of vabicaserin and compare it to risperidone.
Age
20 - 65 years
Sex
ALL
Healthy Volunteers
No
Start Date
November 1, 2008
Primary Completion Date
July 1, 2009
Completion Date
July 1, 2009
Last Updated
January 29, 2013
SCA-136 50mg/day
DRUG
SCA-136 150 mg/day
DRUG
SCA-136 300mg/day
DRUG
Risperidone 4mg/day
DRUG
Lead Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
NCT07455929
NCT06740383
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