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临床试验/CTRI/2011/07/001859
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

发起方
BIAL Portela Ca SA

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