An Open-Label Extension Trial to Assess the Safety of Long-Term Treatment of Rotigotine in Advance-Stage Parkinson's Disease
Completed · Phase 3
Conditions studied: Parkinson's Disease
In brief
The objective of this open-label extension is to assess the safety and tolerability of long-term treatment of the Rotigotine patch in subjects with advanced-stage idiopathic Parkinson's Disease.
Key facts
- Study ID
- NCT00594386
- Run by
- UCB Pharma
- People needed
- 258
- Starts
- 2002-08-01
- Expected to finish
- 2008-12-01
- Last updated by the study team
- 2014-10-02
Who can join
Age: 31 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subjects who have completed six months of maintenance treatment in the SP650 double-blind trial
You may not qualify if…
- Subjects who had an ongoing serious adverse event from the SP650 double-blind trial that was assessed as related to study medication
Where it is running
- Study site — Huntsville, Alabama, United States
- Study site — Peoria, Arizona, United States
- Study site — Phoenix, Arizona, United States
- Study site — Tucson, Arizona, United States
- Study site — Hot Springs, Arkansas, United States
- Study site — Fountain Valley, California, United States
- Study site — Fresno, California, United States
- Study site — Irvine, California, United States
- Study site — Los Angeles, California, United States
- Study site — Danbury, Connecticut, United States
- Study site — Fairfield, Connecticut, United States
- Study site — New Haven, Connecticut, United States
- Study site — Miami, Florida, United States
- Study site — Pompano Beach, Florida, United States
- Study site — St. Petersburg, Florida, United States
- Study site — Sunrise, Florida, United States
- Study site — Atlanta, Georgia, United States
- Study site — Hoffman Estates, Illinois, United States
- Study site — Fort Wayne, Indiana, United States
- Study site — Kansas City, Kansas, United States
- Study site — Lexington, Kentucky, United States
- Study site — Boston, Massachusetts, United States
- Study site — Southfield, Michigan, United States
- Study site — Minneapolis, Minnesota, United States
- Study site — Henderson, Nevada, United States
Full record on ClinicalTrials.gov
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