Investigational Parkinson's Disease In Patients Not Well Controlled On L-Dopa

This study has been completed.

First Received: September 26, 2006 Last Updated: May 15, 2009 History of Changes

Sponsor:	GlaxoSmithKline
Information provided by:	GlaxoSmithKline
ClinicalTrials.gov Identifier:	NCT00381472

Purpose

The purpose of this double-blind, placebo controlled study is to evaluate the safety and effectiveness of an investigational Parkinson's disease drug in patients with advanced disease who are not well-controlled on their L-dopa medication.

Condition	Intervention	Phase
Parkinson's Disease	Drug: Ropinirole	Phase III

Study Type:	Interventional
Study Design:	Treatment, Randomized, Double-Blind, Parallel Assignment, Safety/Efficacy Study
Official Title:	A Phase III, Randomised, Double-Blind, Placebo-Controlled, Parallel Group Study of Six Months Treatment With Ropinirole CR as Adjunctive Therapy in Patients With Parkinson's Disease Who Are Not Optimally Controlled on L-Dopa

Resource links provided by NLM:

Genetics Home Reference related topics: familial paroxysmal nonkinesigenic dyskinesia Parkinson disease

MedlinePlus related topics: Parkinson's Disease

Drug Information available for: Levodopa Ropinirole hydrochloride Ropinirole

U.S. FDA Resources

Further study details as provided by GlaxoSmithKline:

Primary Outcome Measures:

Mean change from baseline in awake time "off" at Week 24 LOCF (last observation carried forward).

Secondary Outcome Measures:

Mean change from baseline in:
amount and percent of awake time spent "on"
percent awake time spent "off"
Unified Parkinson's Disease Rating Scale (UPDRS) total motor score
UPDRS Activities of Daily Living score

Estimated Enrollment:	393
Study Start Date:	June 2003

Eligibility

Ages Eligible for Study:	30 Years and older
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

Idiopathic Parkinson's disease
Modified Hoehn and Yahr Scale Stages II - IV
Stable dose of L-dopa for at least 4 weeks prior to screening.
Lack of control with L-dopa therapy.
Women of child-bearing potential must use a clinically accepted form of birth control.

Exclusion Criteria:

Significant and/or uncontrolled medical conditions (excluding Parkinson's disease) within 3 months of screening.
Any abnormality, at screening, that is considered clinically relevant by the Investigator.
Dementia
Use of dopamine agonists within 4 weeks of screening visit.
Participation in other investigational drug studies.

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00381472

Show 75 Study Locations

Sponsors and Collaborators

GlaxoSmithKline

Investigators

Study Director:

GSK Clinical Trials, MD

GlaxoSmithKline

More Information

No publications provided

Responsible Party:	GSK ( Study Director )
Study ID Numbers:	101468/169
Study First Received:	September 26, 2006
Last Updated:	May 15, 2009
ClinicalTrials.gov Identifier:	NCT00381472 History of Changes
Health Authority:	United States: Food and Drug Administration

Keywords provided by GlaxoSmithKline:

Parkinson's Disease
Adjunctive Therapy with L-dopa
Dyskinesia

Additional relevant MeSH terms:

Neurotransmitter Agents
Levodopa
Ropinirole
Molecular Mechanisms of Pharmacological Action
Anti-Dyskinesia Agents
Physiological Effects of Drugs
Basal Ganglia Diseases
Nervous System Diseases
Central Nervous System Diseases
Antiparkinson Agents

Dopamine Agonists
Brain Diseases
Neurodegenerative Diseases
Pharmacologic Actions
Parkinson Disease
Movement Disorders
Therapeutic Uses
Dopamine Agents
Parkinsonian Disorders
Central Nervous System Agents

ClinicalTrials.gov processed this record on November 09, 2009