NCT01023282已完成1 期
Randomised, Double-blind, Placebo-controlled Study Evaluating Safety and Tolerability of ACR325 in Parkinson's Disease Patients, With Evaluation of the Effect on Levodopa Induced Dyskinesias as a Secondary Measure
NeuroSearch A/S2 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2009年11月最近更新:
适应症
干预措施
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 22
- 试验地点
- 2
- 主要终点
- Safety and tolerability
研究概览
简要总结
The study will evaluate the safety and tolerability of ACR325 in Parkinson disease patients and evaluate the effect on levodopa induced dyskinesias.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 30 Years 至 75 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Diagnosis of idiopathic Parkinson"s disease according to the United Kingdom Parkinson's Disease Society brain bank diagnostic criteria
- •Levodopa induced dyskinesia
排除标准
- •Previous surgery for Parkinson's disease
- •Any current or history of heart condition or increased pro-arrhythmic risk
- •Severe or ongoing unstable medical condition
研究组 & 干预措施
ACR325
Experimental
干预措施: ACR325 (Drug)
Placebo
Placebo Comparator
干预措施: ACR325 (Drug)
Placebo
Placebo Comparator
干预措施: Placebo (Drug)
结局指标
主要结局
Safety and tolerability
时间窗: 4 weeks
次要结局
未报告次要终点
研究者
研究点 (2)
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