Fit-for-purpose method development and validation for successful biomarker measurement

被引:518
|
作者
Lee, JW
Devanarayan, V
Barrett, YC
Weiner, R
Allinson, J
Fountain, S
Keller, S
Weinryb, I
Green, M
Duan, L
Rogers, JA
Millham, R
O'Brien, PJ
Sailstad, J
Khan, M
Ray, C
Wagner, JA
机构
[1] MDS Pharma Serv, Lincoln, NE USA
[2] Merck & Co Inc, Blue Bell, PA USA
[3] Bristol Myers Squibb Co, Princeton, NJ 08543 USA
[4] BAS Analyt Ltd, Kenilworth, England
[5] Pfizer Global Res & Dev, Ann Arbor, MI USA
[6] Prot Design Labs Inc, Fremont, CA USA
[7] Wyeth Res, Collegeville, PA USA
[8] Millenium Pharmaceut, Cambridge, MA USA
[9] Quest Pharmaceut Serv, Newark, DE USA
[10] Pfizer Global Res & Dev, Groton, CT USA
[11] Therakos Inc, Exton, PA USA
[12] Trimeris Inc, Morrisville, NC USA
[13] Covance Labs Inc, Chantilly, VA USA
[14] Eli Lilly & Co, Indianapolis, IN 46285 USA
[15] Merck & Co Inc, Rahway, NJ 07065 USA
关键词
assay validation; biomarkers; drug development; fit-for-purpose method development and validation;
D O I
10.1007/s11095-005-9045-3
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Despite major advances in modern drug discovery and development, the number of new drug approvals has not kept pace with the increased cost of their development. Increasingly, innovative uses of biomarkers are employed in an attempt to speed new drugs to market. Still, widespread adoption of biomarkers is impeded by limited experience interpreting biomarker data and an unclear regulatory climate. Key differences preclude the direct application of existing validation paradigms for drug analysis to biomarker research. Following the AAPS 2003 Biomarker Workshop (J. W. Lee, R. S. Weiner, J. M. Sailstad, et al. Method validation and measurement of biomarkers in nonclinical and clinical samples in drug development. A conference report. Pharm Res 22:499-511, 2005), these and other critical issues were addressed. A practical, iterative, "fit-for-purpose" approach to biomarker method development and validation is proposed, keeping in mind the intended use of the data and the attendant regulatory requirements associated with that use. Sample analysis within this context of fit-for-purpose method development and validation are well suited for successful biomarker implementation, allowing increased use of biomarkers in drug development.
引用
收藏
页码:312 / 328
页数:17
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