Method validation and measurement of biomarkers in nonclinical and clinical samples in drug development: A conference report

被引:124
作者
Lee, JW [1 ]
Weiner, RS
Sailstad, JM
Bowsher, RR
Knuth, DW
O'Brien, PJ
Fourcroy, JL
Dixit, R
Pandite, L
Pietrusko, RG
Soares, HD
Quarmby, V
Vesterqvist, OL
Potter, DM
Witliff, JL
Fritche, HA
O'Leary, T
Perlee, L
Kadam, S
Wagner, JA
机构
[1] MDS Pharma Serv, Lincoln, NE USA
[2] Bristol Myers Squibb Co, Princeton, NJ USA
[3] Trimeris Inc, Durham, NC USA
[4] LINCO Diagnost Serv, St Charles, MO USA
[5] Jasper Clin, Kalamazoo, MI USA
[6] Eli Lilly & Co, Indianapolis, IN 46285 USA
[7] Walter Reed Army Med Ctr, Bethesda, MD USA
[8] Merck & Co Inc, West Point, PA USA
[9] GlaxoSmithKline, Res Triangle Pk, NC USA
[10] Millennium Pharmaceut Inc, Cambridge, MA USA
[11] Pfizer Global Res, Groton, CT USA
[12] Genetech Inc, San Francisco, CA USA
[13] Univ Louisville, Louisville, KY 40292 USA
[14] Univ Texas, MD Anderson Hosp, Austin, TX 78712 USA
[15] US FDA, Rockville, MD 20857 USA
[16] Mol Staging Inc, New Haven, CT USA
关键词
biomarkers; nonclinical and clinical drug development; quantitative method development and validation;
D O I
10.1007/s11095-005-2495-9
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Biomarkers are increasingly used in drug development to aid scientific and clinical decisions regarding the progress of candidate and marketed therapeutics. Biomarkers can improve the understanding of diseases as well as therapeutic and off-target effects of drugs. Early implementation of biomarker strategies thus promises to reduce costs and time-to-market as drugs proceed through increasingly costly and complex clinical development programs. The 2003 American Association of Pharmaceutical Sciences/Clinical Ligand Assay Society Biomarkers Workshop (Salt Lake City, UT, USA, October 24-25, 2003) addressed key issues in biomarker research, with an emphasis on the validation and implementation of biochemical biomarker assays, covering from preclinical discovery of efficacy and toxicity biomarkers through clinical and postmarketing implementation. This summary report of the workshop focuses on the major issues discussed during presentations and open forums and noted consensus achieved among the participants on topics from nomenclature to best practices. For example, it was agreed that because reliable and accurate data provide the basis for sound decision making, biomarker assays must be validated in a manner that enables the creation of such data. The nature of biomarker measurements often precludes direct application of regulatory guidelines established for clinical diagnostics or drug bioanalysis, and future guidance on biomarker assay validation should therefore be adaptable enough that validation criteria do not stifle creative biomarker solutions.
引用
收藏
页码:499 / 511
页数:13
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