Update to the European Bioanalysis Forum recommendation on biomarkers assays; bringing context of use into practice

Author:

Goodman Joanne1,Cowan Kyra J2,Golob Michaela3,Karlsson Lars4,Kunz Ulrich5,Nelson Robert6,Ulrichts Hans7,Stevenson Lauren8,Terry Linda9,Timmerman Philip10

Affiliation:

1. Clinical Pharmacology & Safety Sciences, R&D, AstraZeneca, Cambridge CB21 6GH, UK

2. Drug Metabolism & Pharmacokinetics, R&D, Merck KGaA, Darmstadt 64293, Germany

3. Bioanalysis, Nuvisan GmbH, Neu-Ulm 89231, Germany

4. Translational Medicine, R&D, Ferring Pharmaceuticals, Copenhagen 2300, Denmark

5. Translational Medicine & Clinical Pharmacology, Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach 88400, Germany

6. Science & Innovation, Covance Laboratories, Meyrin, Geneva 1217, Switzerland

7. Translational Biomarkers & Bioanalysis, R&D, UCB Pharma, Braine l'Alleud 1420, Belgium

8. Immunologix Laboratories, Tampa, FL 33634, USA

9. Department of Bioanalysis, Immunogenicity & Biomarkers, GlaxoSmithKline R&D, Stevenage SG1 2NY, UK

10. European Bioanalysis Forum vzw (EBF), Havenlaan 86c b204, Brussels 1000, Belgium

Abstract

In 2012, the European Bioanalysis Forum published a recommendation on biomarker method development and the bioanalysis of biomarkers in support of drug development. Since then, there has been significant discussion on how to bring the topic of context of use of biomarker assays to the forefront so that the purpose of the assay, the use of the data and the decisions being made with the data are well defined and clearly understood, not just by the bioanalytical scientist, but across all stakeholders. Therefore, it is imperative that discussions between the bioanalytical laboratory and the end users of the data happen early (and regularly) in the drug development process to enable the right assays to be developed and appropriately validated to generate the correct data and allow suitable decisions to be made. This updated refinement to the previous European Bioanalysis Forum recommendation will highlight the items to consider when discussing context of use for biomarker assay development and validation, thus enabling the correct conversations to occur and the move away from the misapplication of PK assay validation criteria to biomarker assays.

Publisher

Future Science Ltd

Subject

Medical Laboratory Technology,Clinical Biochemistry,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Analytical Chemistry

Reference24 articles.

1. FDA-NIH Biomarker Working Group. BEST (Biomarkers, EndpointS, and other Tools) Resource (2016). https://www.ncbi.nlm.nih.gov/books/NBK338448/

2. European Medicines Agency. Guideline on Bioanalytical Method Validation (2011). https://www.ema.europa.eu/en/bioanalytical-method-validation

3. US FDA. Guidance for Industry: Bioanalytical Method Validation (2018). https://www.fda.gov/downloads/drugs/guidances/ucm070107.Pdf

4. Ministry of Health, Labour and Welfare (Japan). Guideline on Bioanalytical Method Validation in Pharmaceutical Development (2013). www.nihs.go.jp/drug/BMV/index.html

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3