advancements in first-in-class therapies and breakthrough technologies.The United States has maintained its leadership in first-in-class therapies and breakthrough technologies,driven by advanced regulatory pathways,s...advancements in first-in-class therapies and breakthrough technologies.The United States has maintained its leadership in first-in-class therapies and breakthrough technologies,driven by advanced regulatory pathways,significant multinational corporation investments,a robust Research and Development(R&D)workforce,and continuous technological innovation.Additionally,global impact of the Food and Drug Administration(FDA)is further amplified through collaborations like Project Orbis,which facilitates simultaneous reviews of cancer treatments by multiple regulatory authorities worldwide.Europe,while historically strong,faces growing challenges in maintaining its competitive edge,particularly due to protracted regulatory timelines and complex coordination among its member states.In this competitive global environment,China has rapidly transformed from a generics-dominated market to a key player in innovative drug development.This article reviews China’s progress in innovative drug R&D from 2019 to 2023,emphasizing regulatory modernization,clinical trial advancements,and the emergence of novel therapies.By comparing China’s developments with above global counterparts,this review highlights the country’s achievements in regulatory efficiency,clinical trial progress,and the development of innovative therapies such as biologics and cell and gene therapies.展开更多
基金supported by the Key Project of the National Medical Products Administration for the Construction of the Drug Regulatory Science System (RS2024Z003).
文摘advancements in first-in-class therapies and breakthrough technologies.The United States has maintained its leadership in first-in-class therapies and breakthrough technologies,driven by advanced regulatory pathways,significant multinational corporation investments,a robust Research and Development(R&D)workforce,and continuous technological innovation.Additionally,global impact of the Food and Drug Administration(FDA)is further amplified through collaborations like Project Orbis,which facilitates simultaneous reviews of cancer treatments by multiple regulatory authorities worldwide.Europe,while historically strong,faces growing challenges in maintaining its competitive edge,particularly due to protracted regulatory timelines and complex coordination among its member states.In this competitive global environment,China has rapidly transformed from a generics-dominated market to a key player in innovative drug development.This article reviews China’s progress in innovative drug R&D from 2019 to 2023,emphasizing regulatory modernization,clinical trial advancements,and the emergence of novel therapies.By comparing China’s developments with above global counterparts,this review highlights the country’s achievements in regulatory efficiency,clinical trial progress,and the development of innovative therapies such as biologics and cell and gene therapies.
