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临床试验/NCT01060878
NCT01060878已完成2 期

Phase II, Randomised, Double-blind, Placebo-controlled Study to Investigate the Efficacy, Safety and Tolerability of PYM50028 in Subjects With Early-stage Parkinson's Disease Administered Once Daily for 28 Weeks

Phytopharm110 个研究点 分布在 3 个国家目标入组 425 人开始时间: 2010年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
425
试验地点
110
主要终点
Unified Parkinson's Disease Rating Scale parts II & III combined score

研究概览

简要总结

A study to test the therapeutic benefit of the compound PYM50028, versus placebo, in treating early-stage Parkinson's disease. Therapeutic benefit will be assessed using the Unified Parkinson's Disease Rating Scale (UPDRS). It is hypothesised that PYM50028 will be safe and well tolerated in this study and demonstrate therapeutic benefit in this patient population.

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
35 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • confirmed diagnosis of early-stage idiopathic PD within the 2 years prior to screening
  • subjects who are not currently receiving any PD treatment

排除标准

  • female of child-bearing potential
  • history of neurosurgical procedures for PD
  • history of severe psychiatric illness

研究组 & 干预措施

Dose II

Experimental

干预措施: PYM50028 (Drug)

Dose I

Experimental

干预措施: PYM50028 (Drug)

Dose III

Experimental

干预措施: PYM50028 (Drug)

Placebo

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

Unified Parkinson's Disease Rating Scale parts II & III combined score

时间窗: 28 Weeks

次要结局

未报告次要终点

研究者

发起方
Phytopharm
申办方类型
Industry
责任方
Sponsor

研究点 (110)

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