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| 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
| Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations |
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| Significant events and approaches for the overall study following participant enrollment, but prior to group assignment |
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| 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) |
| Ropinirole PR/XR | |
|---|---|
| STARTED | 62 |
| COMPLETED | 42 |
| NOT COMPLETED | 20 |
| Adverse Event | 14 |
| Lack of Efficacy | 2 |
| Withdrawal by Subject | 4 |
Baseline Characteristics
| 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) |
| Ropinirole PR/XR | |
|---|---|
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Number of Participants
[units: participants] |
62 |
|
Age
[units: years] Mean ± Standard Deviation |
67.2 ± 8.05 |
|
Gender
[units: participants] |
|
| Female | 37 |
| Male | 25 |
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Race/Ethnicity, Customized
[units: participants] |
|
| Asian – Japanese Heritage | 62 |
Outcome Measures
| 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 ] |
More Information
| 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:
|
| 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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| 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 |