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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

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UCB

Status and phase

Completed
Phase 3

Conditions

Parkinson's Disease

Treatments

Drug: PARCOPA

Study type

Interventional

Funder types

Industry

Identifiers

Details and patient eligibility

About

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.

Full description

See approved Package Insert for Adverse Event information.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Stable Parkinson's Disease

Exclusion criteria

  • Not using carbidopa/levodopa tablets

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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