Wagner John A
Department of Clinical Pharmacology, Merck Research Laboratories, Merck & Co. Inc., Rahway, NJ 07065, USA.
Annu Rev Pharmacol Toxicol. 2008;48:631-51. doi: 10.1146/annurev.pharmtox.48.113006.094611.
The strategic, fit-for-purpose use of the combination of robust target engagement and well-qualified disease-related biomarkers enhances understanding of the mechanism of action, ties together preclinical and clinical data, enables the assessment of target engagement, facilitates early proof of concept and dose focusing, and increases the efficiency of early clinical development with improved quality of decision making. Significant progress in biomarker discovery, validation, and qualification has increased drug-development decision making and regulatory applications. Target engagement biomarkers are present early in a pathophysiologic cascade and inform on physical or biological interactions with the molecular target of the drug. Disease-related biomarkers are present late in the pathophysiologic cascade and are linked to clinical benefit; thus, they assess a drug's effect on a particular disease. Together, these concepts lay the groundwork for high-quality drug-development decision making and a framework for the acceptance and qualification of biomarkers for regulatory use.
将强大的靶点结合与资质良好的疾病相关生物标志物相结合进行战略性、针对性的运用,可增强对作用机制的理解,将临床前和临床数据联系起来,实现对靶点结合的评估,促进早期概念验证和剂量聚焦,并提高早期临床开发的效率,同时改善决策质量。生物标志物发现、验证和资质认定方面的重大进展增加了药物开发决策和监管应用。靶点结合生物标志物在病理生理级联反应早期出现,并反映与药物分子靶点的物理或生物学相互作用。疾病相关生物标志物在病理生理级联反应后期出现,并与临床获益相关联;因此,它们评估药物对特定疾病的影响。这些概念共同为高质量的药物开发决策奠定了基础,并为监管用途生物标志物的认可和资质认定提供了框架。