Overcoming obstacles in Parkinson's disease

被引:38
|
作者
Sherer, Todd B. [1 ]
Chowdhury, Sohini [1 ]
Peabody, Katherine [1 ]
Brooks, Deborah W. [1 ]
机构
[1] Michael J Fox Fdn Parkinsons Res, Grand Cent Stn, New York, NY 10163 USA
关键词
alpha-synuclein; biomarkers; disease modification; clinical trial recruitment; ALPHA-SYNUCLEIN; DOUBLE-BLIND; GENE; MUTATIONS; DYSKINESIA; TRIAL; FAMILIES; RISK;
D O I
10.1002/mds.25260
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Improved symptomatic and disease-modifying treatments are needed for Parkinson's disease (PD). Although significant advances have been made in the understanding of PD etiology, the translation of these discoveries into novel transformative therapies has been limited as a result of systemic challenges in PD drug development. Preclinical testing lacks clear standards and prioritization criteria for advancing therapies to the clinic. Clinical testing is marked by expensive, long, and uninformative studies. In parallel to these scientific challenges, funding of late-stage drug development has become increasingly scarce and risk averse. In this context, novel models of collaboration and funding are opening up new avenues for pursuing treatments. This review will discuss the most critical challenges in PD drug development and the innovative approaches being developed to overcome these hurdles. (C) 2012 Movement Disorder Society
引用
收藏
页码:1606 / 1611
页数:6
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