Princeton, New Jersey 08540

  • Parkinson's Disease

Purpose:

This is a 1-year, open-label, long-term safety extension for patients who have completed prior istradefylline studies 6002-EU-007, 6002-US-013 or 6002-US-018.


Study summary:

Patients with Parkinson's disease with motor complications on levodopa therapy who completed the prior double-blind studies 6002-EU-007, 6002-US-013 or 6002-US-018 are eligible to enter into this 1-year, long-term open safety study with a starting istradefylline dose of 40mg per day.


Criteria:

Inclusion Criteria: - Completion of study 6002-EU-007, 6002-US-013 or 6002-US-018 - Non-pregnant and either not of childbearing potential or using specified contraception Exclusion Criteria: - History of psychotic illness - Variant/atypical Parkinson's disease - Cancer within 5 years of enrollment - ALT/AST levels > 1.5 times ULN - Seizure disorder - Neuroleptic malignant syndrome


NCT ID:

NCT00199368


Primary Contact:

Study Director
Neil Sussman, MD
Kyowa Kirin Pharmaceutical Development, Inc.


Backup Contact:

N/A


Location Contact:

Princeton, New Jersey 08540
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: April 07, 2020

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