Pharmacokinetic/Pharmacodynamic-Driven Drug Development

被引:29
作者
Gallo, James M. [1 ]
机构
[1] Mt Sinai Sch Med, Dept Pharmacol & Syst Therapeut, New York, NY 10029 USA
来源
MOUNT SINAI JOURNAL OF MEDICINE | 2010年 / 77卷 / 04期
关键词
anticancer drugs; drug development; models; pharmacodynamics; pharmacokinetics; PHARMACOKINETIC MODEL; DISCOVERY; DISPOSITION; BRAIN; CLASSIFICATION; BIOMARKERS; GEFITINIB; STRATEGY; FDA;
D O I
10.1002/msj.20193
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The drug discovery and development enterprise, traditionally an industrial juggernaut, has spanned into the academic arena that is partially motivated by the National Institutes of Health Roadmap highlighting translational science and medicine. Because drug discovery and development represents a pipeline of basic to clinical investigations, it meshes well with the "bench to the bedside" prime directive of translational medicine. The renewed interest in drug discovery and development in academia provides an opportunity to rethink the hiearchary of studies with the hope of improving the staid approaches that have been criticized for lacking innovation. One area that has received limited attention concerns the use of pharmacokinetic and pharmacodynamic studies in the drug-development process. Using anticancer drug development as a focus, this review will address past and current deficencies in how pharmacokinetic/pharmacodynamic studies are conducted and offer new strategies that might bridge the gap between preclinical and clinical trials. Mt Sinai J Med 77:381-388, 2010. (C) 2010 Mount Sinai School of Medicine
引用
收藏
页码:381 / 388
页数:8
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