12-Week, Double-Blind, Placebo-Controlled, Randomized Study of the Efficacy of 40 mg/Day KW-6002 in Parkinson's Disease Patients on Levodopa/Carbidopa

A 12-week, double-blind, placebo-controlled, multicenter, randomized study designed to
evaluate the safety and efficacy of 40 mg/day istradefylline compared with placebo in
subjects with OFF phenomena advanced PD who were treated with levodopa/carbidopa.

Inclusion Criteria:

1. United Kingdom Parkinson's Disease Society brain bank diagnostic criteria (step 1 and
2).

2. Modified Hoehn and Yahr Scale II-IV in the OFF state.

3. Treated with levodopa/carbidopa for 1 year with a stable regimen for 4 weeks prior to
randomization.

4. Taking at least 4 doses of levodopa (3 doses if at least 2 doses containing slow
release formulation) per day with predictable end of dose wearing off.

5. Successfully completed Parkinson's disease patient diary training with at least 120
minutes of OFF time per day.

6. Stable regimen of other antiparkinson's disease medications for at least 4 weeks
prior to randomization.

7. At least 30 years of age and able to give written informed consent.

Exclusion Criteria:

1. Treatment with liquid levodopa/carbodopa within 4 weeks of randomization.

2. Treatment with MAO inhibitors except selegiline.

3. Treatment with centrally acting dopamine antagonists within 3 months (6 months for
depot preparations), e.g., antipsychotic neuroleptics, metoclopramide, buspirone,
amoxapine.

4. Neurosurgical surgery for Parkinson's disease.

5. Atypical parkinsonism or secondary parkinsonism variants.

6. Diagnosis of cancer or evidence of continued cancer within 5 years of enrollment or
clinically significant illness of any organ system (e.g., ALT or AST > 1.5 times the
upper limit of normal).

7. Mini-Mental Status Examination score of 25 or less.

8. History of drug or alcohol abuse or dependence within 2 years.

9. History of psychotic illness or seizures.

10. Current clinically relevant depression disorder.

11. History of neuroleptic malignant syndrome.

12. Pregnant or lactating females. Women of child-bearing potential must use reliable
method of contraception.