Sarizotan HC1 in Patients With Parkinson's Disease Suffering From Treatment-associated Dyskinesia
| Status: | Completed |
|---|---|
| Conditions: | Parkinsons Disease |
| Therapuetic Areas: | Neurology |
| Healthy: | No |
| Age Range: | 30 - Any |
| Updated: | 7/27/2018 |
| Start Date: | September 30, 2004 |
| End Date: | February 28, 2006 |
A Double-blind, Placebo-controlled, Multicenter, Multinational Phase III Study to Evaluate the Safety and Efficacy of Sarizotan HCl 1 mg b.i.d. in Patients With Parkinson's Disease Suffering From Treatment-associated Dyskinesia
The purpose of this study is to determine if Sarizotan HC1 1 mg b.i.d. (taken twice a day) is
effective in the treatment of dyskinesia associated with dopaminergic treatment of
Parkinson's disease (PD).
effective in the treatment of dyskinesia associated with dopaminergic treatment of
Parkinson's disease (PD).
Inclusion Criteria:
- The subject is an out-patient.
- The subject presents with a diagnosis of idiopathic Parkinson's disease.
- Prior therapy with all registered Parkinsonian medication is allowed.
Exclusion Criteria:
- (For female subjects) The subject is pregnant or lactating.
- The subject is participating in another clinical study or has done so within the past
30 days.
- The subject has received neurosurgical intervention related to PD.
- The subject has relevant renal impairment.
- The subject has relevant hepatic impairment.
- The subject is suffering from any dementia or psychiatric illness.
- The subject has a history of allergic asthma.
We found this trial at
29
sites
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