A new approach to disease-modifying drug trials in Parkinson's disease

被引:11
作者
Barker, Roger A. [1 ]
Stacy, Mark [2 ]
Brundin, Patrik [3 ,4 ]
机构
[1] Univ Cambridge, Cambridge Ctr Brain Repair, Dept Neurol & Clin Neurosci, Cambridge, England
[2] Duke Univ, Sch Med, Durham, NC USA
[3] Van Andel Inst, Ctr Neurodegenerat Sci, Grand Rapids, MI 49503 USA
[4] Lund Univ, Neuronal Survival Unit, Dept Expt Med Sci, Wallenberg Neurosci Ctr, Lund, Sweden
关键词
DOUBLE-BLIND; RECEPTOR STIMULATION; GENE-THERAPY; DELAYED-START; RODENT MODELS; BRAIN; PROGRESSION; RASAGILINE; LEVODOPA;
D O I
10.1172/JCI69690
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Translating new findings in the laboratory into therapies for patients is a slow and expensive process. The development of therapies for neurodegenerative diseases is further complicated by the difficulty in determining whether the drug truly retards the slow degenerative process or provides only symptomatic benefit. In this issue, Aviles-Olmos et al. describe a first in Parkinson's disease (PD) patient study using a drug previously approved for diabetes treatment. In addition to suggesting that the drug may indeed be disease modifying in PD, their innovative approach suggests there may be more rapid and inexpensive avenues for testing novel therapies in PD.
引用
收藏
页码:2364 / 2365
页数:2
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