4.5 Review

Challenges in detecting disease modification in Parkinson's disease clinical trials

期刊

PARKINSONISM & RELATED DISORDERS
卷 32, 期 -, 页码 1-11

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.parkreldis.2016.07.019

关键词

-

向作者/读者索取更多资源

Despite the wealth of encouraging data from numerous compounds that demonstrate neuroprotection in pre-clinical studies of Parkinson's disease, and despite numerous clinical trials, to date, no intervention has been demonstrated to able to modify the course of disease progression. While this failure to translate is likely due to numerous factors including our incomplete understanding of the pathogenic mechanisms underlying PD together with excessive reliance on data from the toxin-based animal models of PD, here we will discuss the structural issues pertaining to inadequate clinical trial design, selection of inappropriate endpoints and poor patient selection which are often not addressed following failed disease modification trials. Future directions to overcome these challenges such as reducing the heterogeneity of patient cohorts, identifying and utilising a pre-diagnostic population, embracing a personalised medicine approach and utilising novel trial designs may be required to ultimately fulfil the goal of conclusively demonstrating evidence of disease modification. (C) 2016 Elsevier Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据