Krishna Rajesh, Herman Gary, Wagner John A
Department of Clinical Pharmacology, Merck Research Laboratories, Merck & Co., Inc., Rahway, New Jersey, USA.
AAPS J. 2008 Jun;10(2):401-9. doi: 10.1208/s12248-008-9041-8. Epub 2008 Aug 7.
The leveraged use of biomarkers presents an opportunity in understanding target engagement and disease impact while accelerating drug development. For effective integration in drug development, it is essential for biomarkers to aid in the elucidation of mechanisms of action and disease progression. The recent years have witnessed significant progress in biomarker selection, validation, and qualification, while enabling surrogate and clinical endpoint qualification and application. Biomarkers play a central role in target validation for novel mechanisms. They also play a central role in the learning/confirming paradigm, particularly when utilized in concert with pharmacokinetic/pharmacodynamic modeling. Clearly, these attributes make biomarker integration attractive for scientific and regulatory applications to new drug development. In this review, applications of proximal, or target engagement, and distal, or disease-related, biomarkers are highlighted using the example of the recent development of sitagliptin for type 2 diabetes, wherein elucidation of target engagement and disease-related biomarkers significantly accelerated sitagliptin drug development. Importantly, use of biomarkers as tools facilitated design of clinical efficacy trials while streamlining dose focus and optimization, the net impact of which reduced overall cycle time to filing as compared to the industry average.
生物标志物的杠杆式应用为理解靶点参与情况和疾病影响提供了契机,同时能加速药物研发。为有效整合到药物研发中,生物标志物有助于阐明作用机制和疾病进展至关重要。近年来,生物标志物的选择、验证和鉴定取得了显著进展,同时也使替代终点和临床终点的鉴定及应用成为可能。生物标志物在新机制的靶点验证中发挥着核心作用。它们在学习/确证范式中也发挥着核心作用,尤其是与药代动力学/药效学模型协同使用时。显然,这些特性使生物标志物整合在新药研发的科学和监管应用中颇具吸引力。在本综述中,以近期用于2型糖尿病的西格列汀的研发为例,重点介绍了近端(即靶点参与)和远端(即疾病相关)生物标志物的应用,其中对靶点参与和疾病相关生物标志物的阐明显著加速了西格列汀的药物研发。重要的是,将生物标志物用作工具有助于临床疗效试验的设计,同时简化剂量聚焦和优化,其净影响是与行业平均水平相比,减少了总体申报周期。