The drug development crisis: Efficiency and safety

被引:32
作者
Caskey, C. Thomas [1 ]
机构
[1] Univ Texas, Hlth Sci Ctr, Brown Fdn Inst Mol Med Prevent Human Dis, Houston, TX 77030 USA
来源
ANNUAL REVIEW OF MEDICINE | 2007年 / 58卷
关键词
targets; screening; antibodies; NCEs; phase IV;
D O I
10.1146/annurev.med.58.042705.124037
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
Despite advancements in genetics, chemistry, and protein engineering, recent years have seen fewer approvals of new drugs, increases in development costs, and high-profile drug withdrawals. This article focuses on technologic methods for improving drug development efficiency. These technologies include high-content cell screening, expression profiling, mass spectroscopy, mouse models of disease, and a post-launch screening program that enables investigations of adverse drug effects. Implementation of these new technologies promises to improve performance in drug development and safety.
引用
收藏
页码:1 / 16
页数:18
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