Parkinson's Disease Clinical Trial
Official title:
A Multicenter, Open-label Trial to Assess Subject Preference of PARCOPA, Carbidopa/Levodopa Orally Disintegrating Tablets, Compared to Conventional Carbidopa/Levodopa Tablets in Subjects With Stable Parkinson's Disease
| Verified date | September 2009 |
| Source | UCB Pharma |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | United States: Institutional Review Board |
| Study type | Interventional |
The objective of this trial was to assess subject preference for PARCOPA, carbidopa/levodopa Orally Disintegrating Tablets (ODT), compared with conventional carbidopa/levodopa tablets, in subjects with stable Parkinson's disease.
| Status | Completed |
| Enrollment | 0 |
| Est. completion date | May 2004 |
| Est. primary completion date | May 2004 |
| Accepts healthy volunteers | |
| Gender | Both |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Stable Parkinson's Disease Exclusion Criteria: - Not using carbidopa/levodopa tablets |
Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Open Label
| Country | Name | City | State |
|---|---|---|---|
| United States | Schwarz | Milwaukee | Wisconsin |
| Lead Sponsor | Collaborator |
|---|---|
| UCB Pharma |
United States,
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