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Completed Phase 3 Interventional Results available

Trial to Assess Parkinson's Disease (PD) Symptom Control to Four Doses of Rotigotine in a Transdermal Patch

ClinicalTrials.gov ID: NCT00522379

Public ClinicalTrials.gov record NCT00522379. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 18, 2026, 8:21 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Double-blind, Placebo-controlled, 5-arm, Parallel-group Trial to Assess Rotigotine Transdermal System Dose Response in Subjects With Advanced-stage Parkinson's Disease

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to show Rotigotine dose response at four doses of Rotigotine used with L-dopa in treating advanced stage Parkinson's disease.

Study identification

NCT ID
NCT00522379
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
UCB Pharma
Industry
Enrollment
514 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
30 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 2007 (Type not available)
Primary completion
Jul 2011 (Actual)
Completion
Jul 2011 (Actual)
Last update posted
Oct 27, 2014

2007 – 2011

United States locations

U.S. sites
62
U.S. states
29
U.S. cities
62
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed Tuscaloosa Alabama — —
Not listed Gilbert Arizona — —
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Not listed Miami Florida — —
Not listed Naples Florida — —
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Not listed St. Petersburg Florida — —
Not listed Sunrise Florida — —
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Not listed Decatur Georgia — —
Not listed Macon Georgia — —
Not listed Suwanee Georgia — —
Not listed Chicago Illinois — —
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Not listed Greensburg Pennsylvania — —
Not listed Souderton Pennsylvania — —
Not listed Upland Pennsylvania — —
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Not listed Lubbock Texas — —
Not listed San Antonio Texas — —
Not listed Midvale Utah — —
Not listed South Ogden Utah — —
Not listed Alexandria Virginia — —
Not listed Richmond Virginia — —
Not listed Roanoke Virginia — —
Not listed Virginia Beach Virginia — —
Not listed Kirkland Washington — —
Not listed Spokane Washington — —
Not listed Milwaukee Wisconsin — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 15 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00522379, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 27, 2014 · Synced Oct 18, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00522379 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →