Clinical Trials Directory

Trials / Completed

CompletedNCT02610231

Long Term Study of Istradefylline in Subjects With Moderate to Severe Parkinson's Disease

A Phase 3, Long-term, Open-label Study of Istradefylline in Subjects With Moderate to Severe Parkinson's Disease

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
239 (actual)
Sponsor
Kyowa Kirin Co., Ltd. · Industry
Sex
All
Age
30 Years
Healthy volunteers
Not accepted

Summary

This is a Phase 3, 52-week, open-label, flexible-dose, multinational, multicenter study to evaluate the safety and tolerability of istradefylline 20 or 40 mg/d in subjects with moderate to severe PD with motor fluctuations and dyskinesia on levodopa combination (levodopa/carbidopa or levodopa/benserazide) therapy plus at least one adjunctive PD medication. Subjects who completed 12 weeks of double-blind treatment and the 30-day follow-up period in Study No. 6002-014 will undergo Screening and Baseline evaluations for eligibility for the study. Eligible subjects will be treated with istradefylline at a starting dose of 20 mg/d with an option for a dose adjustment to 40 mg/d at Week 12 based on the Investigator's judgment of each subject's response and tolerability. If deemed necessary, one unscheduled dose adjustment visit between Week 2 to Week 12 is allowed in accordance with clinical judgment of the Investigator. Subjects who had a dose adjustment to 40 mg/d can have their dose decreased to 20 mg/d by the Investigator at a second unscheduled dose adjustment visit if there are tolerability issues. The istradefylline dose should remain fixed between Week 26 to Week 52. Consultation with the Sponsor's Medical Monitor is required prior to any unscheduled dose adjustment visits. A subject may discontinue from the study at any time.

Conditions

Interventions

TypeNameDescription
DRUGIstradefylline 20 mg or 40 mgIstradefylline 20 or 40 mg

Timeline

Start date
2015-12-01
Primary completion
2017-12-20
Completion
2017-12-20
First posted
2015-11-20
Last updated
2024-04-25
Results posted
2019-12-13

Locations

55 sites across 8 countries: United States, Canada, Czechia, Germany, Israel, Italy, Poland, Serbia

Source: ClinicalTrials.gov record NCT02610231. Inclusion in this directory is not an endorsement.