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Updated: Apr 28, 2026

Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System
Published on: December 11, 2016
Evaluación cuantitativa de la implementación del desarrollo de fármacos informado por modelos en medicamentos
Jian Li1,2, Zhenlei Wang3, Chunmin Wei1,2
1Center of Drug Evaluation, National Medical Products Administration, Beijing, China.
Abstract:
Model-informed drug development (MIDD) has emerged as a cornerstone paradigm in global pharmaceutical innovation. Historically underutilized in China, MIDD methodologies gained momentum following the National Medical Products Administration's (NMPA) 2020 release of the Model-Informed Drug Development Technical Guideline, which was subsequently augmented by supplementary technical guidelines to systematically promote and institutionalize MIDD adoption. This study conducts a longitudinal analysis of MIDD implementation in China-approved innovative drugs from 2018 to 2024, spanning pre- and post-guideline eras.
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