Gromova Mariya, Vaggelas Annegret, Dallmann Gabriele, Seimetz Diane
Biopharma Excellence GmbH, Munich, Germany.
Biomark Insights. 2020 Dec 8;15:1177271920974652. doi: 10.1177/1177271920974652. eCollection 2020.
Biomarkers are widely used at every stage of drug discovery and development. Utilisation of biomarkers has a potential to make drug discovery, development and approval processes more efficient. An overview of the current global regulatory landscape is presented in this article with particular emphasis on the validation and qualification of biomarkers, as well as legal framework for companion diagnostics. Furthermore, this article shows how the number of approved drugs with at least 1 biomarker used during development (biomarker acceptance) is affected by the recent advances in the biomarker regulations. More than half of analysed approvals were supported by biomarker data and there has been a slight increase in acceptance of biomarkers in recent years, even though the growth is not continuous. For certain pharmacotherapeutic groups, approvals with biomarkers are more common than without. Examples include immunosuppressants, immunostimulants, drugs used in diabetes, antithrombotic drugs, antineoplastic agents and antivirals. As a conclusion, potential benefits, challenges and opportunities of using biomarkers in drug discovery and development in the current regulatory landscape are summarised and discussed.
生物标志物在药物研发的各个阶段都有广泛应用。使用生物标志物有可能提高药物研发、开发和审批流程的效率。本文概述了当前全球监管格局,特别强调了生物标志物的验证和鉴定,以及伴随诊断的法律框架。此外,本文还展示了在研发过程中使用至少一种生物标志物的获批药物数量(生物标志物接受情况)是如何受到生物标志物法规近期进展的影响。超过一半的分析获批药物得到了生物标志物数据的支持,尽管增长并不连续,但近年来生物标志物的接受度略有增加。对于某些药物治疗类别,有生物标志物支持的获批情况比没有生物标志物的更为常见。例子包括免疫抑制剂、免疫刺激剂、糖尿病用药、抗血栓药物、抗肿瘤药物和抗病毒药物。总之,总结并讨论了在当前监管格局下,在药物研发中使用生物标志物的潜在益处、挑战和机遇。