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Completed Phase 3 Interventional Results available

An Open-label Continuation Study Evaluating the Long-term Safety of Extended Release Ropinirole XL (Formerly CR) in Parkinson''s Disease

ClinicalTrials.gov ID: NCT00632736

Public ClinicalTrials.gov record NCT00632736. 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 19, 2026, 1:57 PM EDT

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

Official title

An Open-Label Extension Study With REQUIP (Ropinirole) CR for Subjects From Studies 101468/165, 101468/168 and 101468/169

Brief summary

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

To evaluate the safety profile of ropinirole XL during long-term treatment in subjects with early and advanced Parkinson's disease

Study identification

NCT ID
NCT00632736
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
419 participants

Conditions and interventions

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
Feb 2004 (Type not available)
Primary completion
Mar 2010 (Actual)
Completion
Mar 2010 (Actual)
Last update posted
Mar 23, 2017

2004 – 2010

United States locations

U.S. sites
25
U.S. states
15
U.S. cities
25
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35294 —
GSK Investigational Site Fountain Valley California 92708 —
GSK Investigational Site San Francisco California 94109 —
GSK Investigational Site Englewood Colorado 80110 —
GSK Investigational Site Boca Raton Florida 33486 —
GSK Investigational Site Panama City Florida 32405 —
GSK Investigational Site Port Orange Florida 32127 —
GSK Investigational Site St. Petersburg Florida 33701 —
GSK Investigational Site Tampa Florida 33606 —
GSK Investigational Site Atlanta Georgia 30342 —
GSK Investigational Site Augusta Georgia 30912 —
GSK Investigational Site Glenview Illinois 60025 —
GSK Investigational Site Kansas City Kansas 66160 —
GSK Investigational Site Boston Massachusetts 02215 —
GSK Investigational Site Bingham Farms Michigan 48025 —
GSK Investigational Site Southfield Michigan 48034 —
GSK Investigational Site Traverse City Michigan 49684 —
GSK Investigational Site Albany New York 12205 —
GSK Investigational Site Durham North Carolina 27705 —
GSK Investigational Site Toledo Ohio 43614-5809 —
GSK Investigational Site Philadelphia Pennsylvania 19107 —
GSK Investigational Site Upland Pennsylvania 19013 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Wichita Falls Texas 76301 —
GSK Investigational Site Milwaukee Wisconsin 53233 —

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 50 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00632736, 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 Mar 23, 2017 · Synced Oct 19, 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 NCT00632736 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →