The Uses of Biomarkers in Drug Development

被引:28
|
作者
Hurko, Orest [1 ,2 ]
机构
[1] Wyeth Res, Discovery Translat Res, Collegeville, PA 19426 USA
[2] Univ Dundee, Dundee, Scotland
来源
BIOMARKERS IN BRAIN DISEASE | 2009年 / 1180卷
关键词
brain disease; biomarker; surrogate; VAGAL NERVE-STIMULATION; CLINICAL-TRIALS; ALZHEIMERS-DISEASE; SURROGATE ENDPOINTS; GENE-EXPRESSION; RISK; PHARMACOGENETICS; MORTALITY; TOXICITY; EFFICACY;
D O I
10.1111/j.1749-6632.2009.04946.x
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
Although the value of "surrogate biomarkers" (strictly speaking, those biomarkers that can serve as surrogate primary endpoints in registration trials) is significant, such biomarkers are few. However, "nonsurrogate biomarkers" are increasingly being used to reduce the risks of drug development. Any given biomarker is usually useful for only one of four types of risk reduction: that associated with (1) an inappropriate dosing regimen; (2) enrollment of nonresponsive subjects into clinical trials; (3) an inability to detect an efficacy signal quickly and reliably in chronic disorders; or (4) delayed recognition of potential side effects and/or toxicity. A biomarker suitable for one purpose is usually not suitable for the other three. Although these considerations apply to all drug development, both the need and availability of appropriate biomarkers in each category vary between therapeutic areas. The focus is on diseases of the brain.
引用
收藏
页码:1 / 10
页数:10
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