TY - JOUR
T1 - Clinical and Quantitative Pharmacology Considerations of mRNA Therapeutics and Vaccine Development
T2 - Bridging Translational and Platform Gaps for Enhanced Decision Making
AU - Van, Linh
AU - Chen, Nancy
AU - Miyazawa, Kenji
AU - Zhang, Miao
AU - Landersdorfer, Cornelia B.
AU - Kirkpatrick, Carl M.J.
AU - Pennucci, Jason
AU - Finn, Patrick F.
AU - Ward, Christine
AU - Gao, Wei
N1 - Publisher Copyright:
© 2025 The Author(s). Clinical Pharmacology & Therapeutics © 2025 American Society for Clinical Pharmacology and Therapeutics.
PY - 2025/12
Y1 - 2025/12
N2 - 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.
AB - 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.
UR - https://www.scopus.com/pages/publications/105019066352
U2 - 10.1002/cpt.70085
DO - 10.1002/cpt.70085
M3 - Review Article
C2 - 41085467
AN - SCOPUS:105019066352
SN - 0009-9236
VL - 118
SP - 1297
EP - 1312
JO - Clinical Pharmacology & Therapeutics
JF - Clinical Pharmacology & Therapeutics
IS - 6
ER -