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NCT00139867 · ClinicalTrials.gov registry record · 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

A Phase 3 study of Parkinson's Disease, sponsored by UCB Pharma.

Completed
Registry status
Phase 3
Development phase
1
Study location

NCT00139867: Completed Phase 3 study of Parkinson's Disease, sponsored by UCB Pharma.

NCT00139867 is a Phase 3 study of Parkinson's Disease that has completed, run by UCB Pharma. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00139867, a Phase 3 study of Parkinson's Disease, has completed, sponsored by UCB Pharma.

COMPLETED
Registry status
Phase 3
Development phase
1
Study location

Study 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.

Conditions Studied

Interventions

  • DRUG PARCOPA

Study Locations (1)

Wisconsin

  • Schwarz - Milwaukee

Trial Details

FieldValue
Start Date 2004-01
Est. Completion 2004-05
Phase Phase 3
UCB Pharma

100 total trials

What the finished NCT00139867 record still lists

NCT00139867 is an interventional study that assigns participants to a tested intervention. An enrollment target was not published in the registry record, which is common for early-stage or observational entries.

The record links to 1 condition, with Parkinson's Disease appearing as the primary indexed condition, and to 1 intervention - of which PARCOPA is the first listed.

NCT00139867 reports a single indexed study location in Wisconsin.

Frequently Asked Questions

What is clinical trial NCT00139867 about?

NCT00139867 is a clinical study titled "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". 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.

What is the current status of trial NCT00139867?

This trial is currently completed. It is a Phase 3 study. The study started on 2004-01. Estimated completion is 2004-05.

What conditions does trial NCT00139867 study?

This clinical trial studies the following conditions: Parkinson's Disease.

What interventions are being tested in trial NCT00139867?

The interventions under investigation include: PARCOPA (DRUG).

Who is sponsoring clinical trial NCT00139867?

This trial is sponsored by UCB Pharma, which has 100 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00139867 being conducted?

This trial has 1 study location across Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT00139867, the US trial registry maintained by the National Library of Medicine. NCT00139867 (unsized enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.