EUCTR2007-002496-14-FI进行中（未招募）不适用
Effects of single doses of Stalevo 200 and levodopa/carbidopa 200/50 mg on striatal 11C-raclopride binding potential in Parkinson’s disease patients with wearing-off symptoms. An open, randomised, active-controlled, two-period crossover study.
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •1. Male or female patients with idiopathic Parkinson’s disease according to the UK Brain Bank criteria.
- •2. Predictable wearing-off symptoms with a response to standard release levodopa/carbidopa (200/50 mg) during the levodopa challenge test lasting for a minimum of 1.5 h and a maximum of 4 h.
- •3. The magnitude of response (peak effect) in the levodopa challenge test is at least 30%. The magnitude of response is defined to be the difference between the baseline score and the lowest UPDRS III score during the levodopa challenge test.
- •4. Hoehn and Yahr stage of at least 2.0 performed during the ON” state.
- •5. Treatment with at least 4 daily doses of levodopa/DDCI ± entacapone (Comtess® or Stalevo®) with total daily levodopa dose in the range of 400-1200mg.
- •6. Unchanged levodopa/DDCI ± entacapone and other antiparkinsonian medication [dopamine agonists, monoamine oxidase B (MAO-B) inhibitor, amantadine and/or anticholinergics with an approved dose], if any, for at least 2 weeks prior to period I.
- •7. Written informed consent (IC) obtained.
- •8. Age of 45-80 years, inclusive.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1. Secondary or atypical parkinsonism.
- •2. Patients with any unpredictable OFF”-periods.
- •3. Patients with moderate to severe treatment-related peak-dose dyskinesia likely to affect the quality of brain MRI or PET imaging.
- •4. Failure to adequately respond to the levodopa (levodopa/carbidopa 200/50 mg) challenge test with the duration of response lasting less than 1.5 h or more than 4 h.
- •5. Presence of a basal ganglia lesion in the MRI image or any other factor(s) that would make MRI or PET imaging likely to be unsatisfactory.
- •6. Presence of any ferromagnetic objects that would make brain MRI imaging contraindicated.
- •7. Patients with a history of laboratory abnormality consistent with, or clinically significant cardiovascular, pulmonary, gastrointestinal, hepatic, renal, neurological or psychiatric disorder or any other major concurrent illness, which may influence the outcome of the study including the interpretation and usage of MRI and PET images for the study purposes.
- •8. History of neuroleptic malignant syndrome (NMS) and/or non-traumatic rhabdomyolysis, malignant melanoma, narrow-angle glaucoma or pheochromocytoma.
- •9. Severe hepatic impairment.
- •10. Any abnormal ECG finding with clinical relevance.
- •11. Female patients of childbearing potential (menstruating or less than 2 years postmenopausal) if they are not using adequate contraception during the study (defined as hormonal contraception, intrauterine device or surgical sterilization) or female patients who are pregnant or lactating.
- •12. Treatment with cabergoline.
- •13. Concomitant treatment with apomorphine, MAO-A inhibitors or non-selective MAO inhibitors.
- •14. Concomitant treatment with any drugs with antidopaminergic action (e.g. with D2 receptor blocking properties) less than two weeks or within five times the elimination half-life of a given drug prior to the first study drug administration. As an exception, the use of domperidone is allowed.
- •15. Current, regular use of any iron preparation that cannot be interrupted for the duration of the study
- •16. Patients who are likely to need a rescue dose of levodopa after the withdrawal from their own levodopa/DDCI ± entacapone medication prior to PET imaging.
- •17. Known hypersensitivity to active study drug substances or to any of the excipients.
- •18. Participation in other drug studies within 30 days prior to study entry.
- •19. Blood donation or loss of significant amount of blood within 60 days prior to the screening.
- •20. Any other condition that in the opinion of the investigator could create a hazard to the subject safety, endanger the study procedures or interfere with the interpretation of study results.
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