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系统药理学
临床药理学
药物开发
计算生物学
转化医学
从长凳到床边
桥接(联网)
转化研究
医学
计算机科学
药物发现
药理学
生物医学
药代动力学
生物信息学
转化式学习
精密医学
人口
安全药理学
模式
系统生物学
临床实习
数据科学
药品
作者
Linh Van,Nancy Chen,Kenji Miyazawa,Miao Zhang,Cornelia B. Landersdorfer,Carl M. J. Kirkpatrick,Jason Pennucci,Patrick F. Finn,Christine K. Ward,Wei Gao
摘要
Messenger RNA (mRNA) technology has emerged as a transformative modality in modern therapeutics and vaccine development, offering a versatile platform for targeted protein expression. This manuscript proposes a clinical and quantitative pharmacology framework to facilitate the development of mRNA therapies from preclinical research to clinical development. We discuss the unique pharmacological and ADME properties of mRNA and its lipid nanoparticle (LNP) delivery system, along with key bioanalytical and regulatory considerations. Specific clinical pharmacology strategies and quantitative approaches are illustrated through real-world examples in oncology, rare metabolic diseases, and vaccines. Finally, we propose a forward-looking clinical and quantitative pharmacology framework that integrates translational modeling, population modeling, physiological-based pharmacokinetic (PBPK), quantitative systems pharmacology (QSP), and Artificial Intelligence (AI)/Machine Learning (ML)-assisted predictive modeling. This integrated approach aims to build platform knowledge of mRNA-based therapies and inform decision making across the drug discovery and development lifecycle in an evolving regulatory landscape.
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