A Study of Istradefylline (KW-6002) for the Treatment of Parkinson's Disease in Patients Taking Levodopa



Status:Completed
Conditions:Parkinsons Disease
Therapuetic Areas:Neurology
Healthy:No
Age Range:30 - Any
Updated:7/14/2016
Start Date:June 2004
End Date:January 2006

Use our guide to learn which trials are right for you!

A 12-week, Double Blind, Placebo-controlled, Randomized, Parallel Group, Multicenter, Fixed Dose Study to Evaluate the Efficacy and Safety of a 20 mg/d Oral Dose of KW-6002 (Istradefylline) as Treatment for Parkinson's Disease in Patients With Motor Response Complications on Levodopa/Carbidopa Therapy.

To establish the efficacy of a 20 mg/day dose of istradefylline for reducing the percentage
of OFF time in patients with advanced Parkinson's disease (PD) treated with levodopa.

To establish the efficacy of a 20 mg/d dose of istradefylline for reducing the percentage of
OFF time in patients with advanced Parkinson's disease (PD) treated with levodopa. Patients
who meet entry criteria will be randomized in a 1 to 1 ratio to either istradefylline or
matching placebo. Patients will be treated for 12 weeks and will have interim visits and end
of treatment visit to assess the efficacy and safety of istradefylline as compared to
placebo.

Inclusion Criteria:

1. UK Parkinson's Disease Society (UKPDS) brain bank criteria (Step 1 and 2) for PD.

2. PD stages 2-4 in the OFF state for Modified Hoehn and Yahr Scale.

3. On levodopa/carbidopa for at least one year, stable dose in past 4 weeks.

4. Currently take at least three doses of levodopa/carbidopa per day.

5. Predictable end of dose wearing off.

6. Able to satisfactorily complete Hauser version of a Parkinson's diary.

7. Have an average of 180 minutes of OFF time on two 24 hour diaries.

8. Be at least 30 years of age.

Exclusion Criteria:

1. Neurosurgical treatment for PD.

2. History of psychosis.

3. Diagnosis of atypical parkinsonism, secondary parkinsonism variant or Parkinson's
plus syndromes.

4. Diagnosis of cancer within 5 years.

5. Mini-mental status examination score of 25 or less.

6. History of seizures or neurologic malignant_syndrome.

7. Clinical depression.
We found this trial at
1
site
Princeton, New Jersey 08540
?
mi
from
Princeton, NJ
Click here to add this to my saved trials