Qualification of translational safety biomarkers.

IF 2.7
John-Michael Sauer, Amy C Porter
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引用次数: 3

Abstract

Safety biomarkers are important drug development tools, both preclinically and clinically. It is a straightforward process to correlate the performance of nonclinical safety biomarkers with histopathology, and ideally, the biomarker is useful in all species commonly used in safety assessment. In clinical validation studies, where histopathology is not feasible, safety biomarkers are compared to the response of standard biomarkers and/or to clinical adjudication. Worldwide, regulatory agencies have put in place processes to qualify biomarkers to provide confidence in the manner of use and interpretation of biomarker data in drug development studies. This paper describes currently qualified safety biomarkers which can be utilized to monitor for nephrotoxicity and cardiotoxicity and ongoing projects to qualify safety biomarkers for liver, skeletal muscle, and vascular injury. In many cases, the development and use of these critical drug development tools is dependent upon partnerships and the precompetitive sharing of data to support qualification efforts.

翻译安全性生物标志物的鉴定。
安全性生物标志物是重要的药物开发工具,无论是临床前还是临床。将非临床安全性生物标志物的性能与组织病理学相关联是一个简单的过程,理想情况下,生物标志物可用于所有常用的安全性评估物种。在临床验证研究中,如果组织病理学不可行,则将安全性生物标志物与标准生物标志物和/或临床裁决的反应进行比较。在世界范围内,监管机构已经建立了对生物标记物进行鉴定的程序,以便在药物开发研究中对生物标记物数据的使用和解释方式提供信心。本文介绍了目前合格的可用于监测肾毒性和心脏毒性的安全生物标志物,以及正在进行的用于肝脏、骨骼肌和血管损伤的安全生物标志物的合格项目。在许多情况下,这些关键药物开发工具的开发和使用依赖于伙伴关系和竞争前数据共享,以支持资格认证工作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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