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

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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).


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
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Saint Petersburg, Florida 33713
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