Sarizotan in Participants With Parkinson's Disease Suffering From Treatment Associated Dyskinesia
| Status: | Completed |
|---|---|
| Conditions: | Parkinsons Disease |
| Therapuetic Areas: | Neurology |
| Healthy: | No |
| Age Range: | 30 - Any |
| Updated: | 4/17/2018 |
| Start Date: | September 30, 2004 |
| End Date: | March 31, 2006 |
A Double-Blind, Placebo-Controlled, Multicenter, Multinational Phase III Study to Evaluate the Safety and Efficacy of Sarizotan in Patients With Parkinson's Disease Suffering From Treatment-Associated Dyskinesia
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.
maximal safety and efficacy for treating treatment associated dyskinesia in Parkinson's
disease participants.
Inclusion Criteria:
- 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
Exclusion Criteria:
- (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
We found this trial at
28
sites
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