CTRI/2011/07/001859已完成3 期
Efficacy and Safety of BIA 9-1067 in Idiopathic Parkinsons Disease Patients With Wearing-off Phenomenon Treated With Levodopa Plus a Dopa Decarboxylase Inhibitor (DDCI): a Double-blind, Randomised, Placebo-controlled, Parallel-group, Multicentre Clinical Study.
BIAL Portela Ca SA0 个研究点目标入组 405 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 405
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1. Able to comprehend and willing to sign an informed consent form.
- •2. Male and female subjects between 30 and 83 years old, inclusive.
- •3. Diagnosed with idiopathic PD according to the UK Parkinsons Disease Society Brain Bank Clinical Diagnostic Criteria (UKPDSBBCDC) for at least 3 years.
- •4. Disease severity Stages I-III (modified Hoehn &Yahr staging) at ON.
- •5. Treated with L-DOPA/DDCI for at least 1 year with clear clinical improvement.
- •6. Treated with 3 to 8 daily doses of L-DOPA/DDCI, which can include a slow-release formulation.
- •7. On a stable regimen of L-DOPA/DDCI and other anti-PD drugs for at least 4 weeks before screening.
- •8. Signs of wearing-off phenomenon (end-of-dose deterioration) for a minimum of 4 weeks before screening with average total daily OFF time while awake of at least 1.5 hours, excluding the early morning pre-first dose OFF, despite optimal anti-PD therapy (based on the investigators judgment.
排除标准
- •1. Non-idiopathic PD (atypical parkinsonism, secondary [acquired or symptomatic] parkinsonism, Parkinson-plus syndrome).
- •2. Dyskinesia disability score 3 in the Unified Parkinsons Disease Rating Scale UPDRS) Sub-section IV A, item 33.
- •3. Severe and/or unpredictable OFF periods.
- •4. Treatment with prohibited medication: entacapone, tolcapone, neuroleptics, venlafaxine, MAO inhibitors (except selegiline up to 10 mg/day in oral formulation or 1.25 mg/day in buccal absorption formulation or rasagiline up to 1mg/day), or antiemetics with antidopaminergic action (except domperidone) within the month before screening.
- •5. Treatment with apomorphine within the month before screening or likely to be needed at any time during the study.
- •6. Dosage change of concomitant anti-PD medication within 4 weeks of screening.
- •7. Previous or planned (during the entire study duration, including the OL period)deep brain stimulation.
- •8. Previous stereotactic surgery (e.g. pallidotomy, thalamotomy) for PD or with planned stereotactic surgery during the study period.
- •9. Any investigational medicinal product (IMP) within the 3 months (or within 5 half-lives, whichever is longer) before screening.
- •10. Any medical condition that might place the subject at increased risk or interfere with assessments.
研究者
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