A Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of Three Doses of Aplindore MR (1, 3 and 6 mg Twice Daily) in Patients with Early Parkinson's Disease

PurposeThis study is being conducted to see whether aplindore is safe, effective and tolerable in the treatment of subjects with the early stages of PD when taken over a period of 90 days. Also, the study will look at how aplindore affects mood, thinking and memory, behavior, impulse control and daytime sleepiness. Aplindore is considered an investigational drug. This means it has not been approved by the U.S. Food and Drug Administration (FDA).
Details Study Number
20082098
Accepts Adults?
Yes
Accepts Children?
No
Fully Enrolled?
No
Contacts Principal Investigator
Roger Kurlan, MD
Contact
Debra Berry, 585-341-7500

For More Information

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