Sarizotan in Participants With Parkinson's Disease Suffering From Treatment Associated Dyskinesia
Completed · Phase 3 · Has a placebo group
Conditions studied: Parkinson's Disease, Dyskinesia
In brief
The purpose of this study is to test multiple doses of sarizotan to establish a dose with maximal safety and efficacy for treating treatment associated dyskinesia in Parkinson's disease participants.
Key facts
- Study ID
- NCT00105521
- Run by
- EMD Serono
- People needed
- 398
- Starts
- 2004-09-30
- Expected to finish
- 2006-03-31
- Last updated by the study team
- 2018-04-02
Who can join
Age: 30 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- The participant is an out-patient
- The participant presents with a diagnosis of idiopathic Parkinson's disease
- Prior therapy with all registered Parkinsonian medication is allowed
You may not qualify if…
- (For female participants) The participant is pregnant or lactating
- The participant is participating in another clinical study or has done so within the past 30 days
- The participant has received neurosurgical intervention related to Parkinson's disease
- The participant has relevant renal impairment
- The participant has relevant hepatic impairment
- The participant is suffering from any dementia or psychiatric illness
- The participant has a history of allergic asthma
Where it is running
- Study site — Phoenix, Arizona, United States
- Study site — Phoenix, Arizona, United States
- Study site — Phoenix, Arizona, United States
- Study site — Scottsdale, Arizona, United States
- Study site — Fayetteville, Arkansas, United States
- Study site — Fountain Valley, California, United States
- Study site — Los Angeles, California, United States
- Study site — Fort Lauderdale, Florida, United States
- Study site — Hollywood, Florida, United States
- Study site — Ocala, Florida, United States
- Study site — Port Charlotte, Florida, United States
- Study site — St. Petersburg, Florida, United States
- Study site — Tampa, Florida, United States
- Study site — Chicago, Illinois, United States
- Study site — Chicago, Illinois, United States
- Study site — Hoffman Estates, Illinois, United States
- Study site — Lexington, Kentucky, United States
- Study site — Baltimore, Maryland, United States
- Study site — Columbia, Maryland, United States
- Study site — Boston, Massachusetts, United States
- Study site — Boston, Massachusetts, United States
- Study site — Golden Valley, Minnesota, United States
- Study site — Omaha, Nebraska, United States
- Study site — Albany, New York, United States
- Study site — New York, New York, United States
Full record on ClinicalTrials.gov
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