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Study Results
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Clinical Evaluation of Ropinirole PR/XR Tablets in Monotherapy for Parkinson's Disease (PD)
This study has been completed.
Study NCT00434304   Information provided by GlaxoSmithKline

First Received on February 9, 2007.   Last Updated on June 30, 2011   History of Changes
Results First Received: November 16, 2009  
Study Type: Interventional
Study Design: Endpoint Classification: Pharmacokinetics Study;   Intervention Model: Single Group Assignment;   Masking: Open Label;   Primary Purpose: Treatment
Conditions: Parkinson Disease
Parkinson's Disease
Intervention: Drug: Ropinirole prolonged release/extended release(PR/XR)

  Participant Flow
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Recruitment Details
Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
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Pre-Assignment Details
Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
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Reporting Groups
  Description
Ropinirole PR/XR Treatment Phase: Fixed titration phase (4 weeks): one tablet of ropinirole PR/XR 2 milligrams (mg) as the initial dose. The dose was titrated weekly by 2 mg/day and was increased to 8 mg/day in Week 4; Flexible titration and maintenance dose phases (48 weeks): from Week 5 up to Week 16, the dose was increased at minimum intervals of 1 week between titration steps (up to 16 mg/day). From Week 16 onward, treatment dose was continuously administered up to Week 52. Taper phase: the dose was tapered over 2 to 3 weeks according to the maintenance dose at completion of the Treatment Phase (or withdrawal)

Participant Flow:   Overall Study
    Ropinirole PR/XR  
STARTED     62  
COMPLETED     42  
NOT COMPLETED     20  
Adverse Event                 14  
Lack of Efficacy                 2  
Withdrawal by Subject                 4  



  Baseline Characteristics
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Reporting Groups
  Description
Ropinirole PR/XR Treatment Phase: Fixed titration phase (4 weeks): one tablet of ropinirole PR/XR 2 milligrams (mg) as the initial dose. The dose was titrated weekly by 2 mg/day and was increased to 8 mg/day in Week 4; Flexible titration and maintenance dose phases (48 weeks): from Week 5 up to Week 16, the dose was increased at minimum intervals of 1 week between titration steps (up to 16 mg/day). From Week 16 onward, treatment dose was continuously administered up to Week 52. Taper phase: the dose was tapered over 2 to 3 weeks according to the maintenance dose at completion of the Treatment Phase (or withdrawal)

Baseline Measures
    Ropinirole PR/XR  
Number of Participants  
[units: participants]
  62  
Age  
[units: years]
Mean ± Standard Deviation
  67.2  ± 8.05  
Gender  
[units: participants]
 
Female     37  
Male     25  
Race/Ethnicity, Customized  
[units: participants]
 
Asian – Japanese Heritage     62  



  Outcome Measures
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1.  Primary:   Food Effects on Cmax and Cmin of SKF101468 (Ropinirole) and Its Metabolites   [ Time Frame: Weeks 5-16 ]

2.  Primary:   Food Effects on AUC0-24 of SKF101468 (Ropinirole) and Its Metabolites   [ Time Frame: Weeks 5-16 ]

3.  Primary:   Food Effects on Tmax of SKF101468 (Ropinirole) and Its Metabolites   [ Time Frame: Weeks 5-16 ]

4.  Primary:   Plasma Trough Concentrations of SKF101468 (Ropinirole) and Its Metabolites   [ Time Frame: Weeks 1-16 ]

5.  Secondary:   Total Score in the Japanese UPDRS Part III   [ Time Frame: Weeks 0-52 ]

6.  Secondary:   Change From Baseline in the Japanese UPDRS Part III   [ Time Frame: Baseline (Week 0) and Weeks 1-52 ]

7.  Secondary:   Percent Change From Baseline in the Japanese UPDRS Part III   [ Time Frame: Baseline (Week 0) and Weeks 1-52 ]

8.  Secondary:   Percentage of Responders of the Total Score in the Japanese UPDRS Total Score in Part III   [ Time Frame: Baseline (Week 0) and Weeks 1-52 ]

9.  Secondary:   Total Score in the Japanese UPDRS Part I   [ Time Frame: Weeks 0-52 ]

10.  Secondary:   Change From Baseline in the Japanese UPDRS Part I   [ Time Frame: Baseline (Week 0) and Weeks 1-52 ]

11.  Secondary:   Percent Change From Baseline in the Japanese UPDRS Part I   [ Time Frame: Baseline (Week 0) and Weeks 1-52 ]

12.  Secondary:   Total Score in the Japanese UPDRS Part II   [ Time Frame: Weeks 0-52 ]

13.  Secondary:   Change From Baseline in the Japanese UPDRS Part II   [ Time Frame: Baseline (Week 0) and Weeks 1-52 ]

14.  Secondary:   Percent Change From Baseline in the Japanese UPDRS Part II   [ Time Frame: Baseline (Week 0) and Weeks 1-52 ]

15.  Secondary:   Total Score in the Japanese UPDRS Part IV   [ Time Frame: Baseline (Week 0) and Weeks 0-52 ]

16.  Secondary:   Change From Baseline in the Japanese UPDRS Part IV   [ Time Frame: Baseline (Week 0) and Weeks 1-52 ]

17.  Secondary:   Percent Change From Baseline in the Japanese UPDRS Part IV   [ Time Frame: Baseline (Week 0) and Weeks 1-52 ]

18.  Secondary:   Summary of the Modified Hoehn & Yahr Criteria Stages   [ Time Frame: Screening-Week 52 ]

19.  Secondary:   Number of Participants Scored as Responders on the Clinician's Global Impression (CGI) Scale   [ Time Frame: Weeks 1-52 ]

20.  Secondary:   Percentage of Participants Who Remained in the Study on the Indicated Days   [ Time Frame: Days 0-364 ]

21.  Secondary:   Change From Baseline in Albumin, Total Protein, and Hemoglobin at Weeks 16 and 52   [ Time Frame: Baseline (Screening) and Weeks 16 and 52 ]

22.  Secondary:   Change From Baseline in Alkaline Phosphatase, Alanine Amino Transferase, Aspartate Amino Transferase, Creatine Kinase, Gamma Glutamyl Transferase, and Lactate Dehydrogenase at Weeks 16 and 52   [ Time Frame: Baseline (Screening) and Weeks 16 and 52 ]

23.  Secondary:   Change From Baseline in Total Bilirubin, Blood Urea Nitrogen, and Creatinine at Weeks 16 and 52   [ Time Frame: Baseline (Screening) and Weeks 16 and 52 ]

24.  Secondary:   Change From Baseline in Blood Urea Nitrogen, Cholesterol, Chloride, Potassium, and Sodium at Weeks 16 and 52   [ Time Frame: Baseline (Screening) and Weeks 16 and 52 ]

25.  Secondary:   Change From Baseline in Prolactin at Weeks 16 and 52   [ Time Frame: Baseline (Screening) and Weeks 16 and 52 ]

26.  Secondary:   Change From Baseline in Hematocrit at Weeks 16 and 52   [ Time Frame: Baseline (Screening) and Weeks 16 and 52 ]

27.  Secondary:   Change From Baseline in Platelet Count and White Blood Cell Count at Weeks 16 and 52   [ Time Frame: Baseline (Screening) and Weeks 16 and 52 ]

28.  Secondary:   Change From Baseline in Red Blood Cell Count at Weeks 16 and 52   [ Time Frame: Baseline (Screening) and Weeks 16 and 52 ]

29.  Secondary:   Urinalysis Data   [ Time Frame: Screening, Week 16, and Week 52 ]

30.  Secondary:   Number of Participants With the Indicated Shift From Baseline in 12-Lead Electrocardiogram (ECG) Findings at Weeks 16 and 52   [ Time Frame: Baseline (Screening) and Weeks 16 and 52 ]

31.  Secondary:   Change From Baseline in Supine and Standing Systolic and Diastolic Blood Pressure at Weeks 16 and 52   [ Time Frame: Baseline (Screening) and Weeks 16 and 52 ]

32.  Secondary:   Change From Baseline in Supine and Standing Pulse Rate at Weeks 16 and 52   [ Time Frame: Baseline (Screening) and Weeks 16 and 52 ]


  Serious Adverse Events
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  Other Adverse Events
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  More Information
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Certain Agreements:  
Principal Investigators are NOT employed by the organization sponsoring the study.
There IS an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.
The agreement is:
unchecked The only disclosure restriction on the PI is that the sponsor can review results communications prior to public release and can embargo communications regarding trial results for a period that is less than or equal to 60 days. The sponsor cannot require changes to the communication and cannot extend the embargo.
unchecked The only disclosure restriction on the PI is that the sponsor can review results communications prior to public release and can embargo communications regarding trial results for a period that is more than 60 days but less than or equal to 180 days. The sponsor cannot require changes to the communication and cannot extend the embargo.


Limitations and Caveats
Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data
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Results Point of Contact:  
Name/Title: GSK Response Center
Organization: GlaxoSmithKline
phone: 866-435-7343


No publications provided


Responsible Party: Cheri Hudson; Clinical Disclosure Advisor, GSK Clinical Disclosure
ClinicalTrials.gov Identifier: NCT00434304     History of Changes
Other Study ID Numbers: ROP106064
Study First Received: February 9, 2007
Results First Received: November 16, 2009
Last Updated: June 30, 2011
Health Authority: Japan: Ministry of Health, Labor and Welfare;   Japan: Pharmaceuticals and Medical Devices Agency