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Clinical Trials/NCT00139867
NCT00139867
Completed
Phase 3

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

UCB Pharma1 site in 1 countryJanuary 2004

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Parkinson's Disease
Sponsor
UCB Pharma
Locations
1
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

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.

Detailed Description

See approved Package Insert for Adverse Event information.

Registry
clinicaltrials.gov
Start Date
January 2004
End Date
May 2004
Last Updated
11 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
UCB Pharma

Eligibility Criteria

Inclusion Criteria

  • Stable Parkinson's Disease

Exclusion Criteria

  • Not using carbidopa/levodopa tablets

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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