Overview

Sarizotan in Participants With Parkinson's Disease Suffering From Treatment Associated Dyskinesia

Status:
Completed
Trial end date:
2006-03-31
Target enrollment:
0
Participant gender:
All
Summary
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.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
EMD Serono
Criteria
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