To assess the tolerability and safety of OPC-14117. To evaluate effects of OPC-14117 on cognitive function, quality of life, and activities of daily living.
Patients receive OPC-14117 or placebo bid for 12 weeks, followed by 12 weeks of open label therapy.
Study Type
INTERVENTIONAL
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
30
Johns Hopkins Hosp
Baltimore, Maryland, United States
Columbia Univ
New York, New York, United States
Univ of Rochester Med Ctr
Rochester, New York, United States
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