4.7 Article

Evolution of drug regulations and regulatory innovation for anticancer drugs in China

期刊

ACTA PHARMACEUTICA SINICA B
卷 12, 期 12, 页码 4365-4377

出版社

INST MATERIA MEDICA, CHINESE ACAD MEDICAL SCIENCES
DOI: 10.1016/j.apsb.2022.08.004

关键词

Regulatory innovations; Drug R&D; Anticancer drugs; Innovative drugs; Expedited program designations; Drug lag; Globalization; Unmet medical need

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China has undergone a revolution in drug regulation over the past two decades, introducing significant changes to accelerate drug review and approvals. This study provides an overview of this revolution and analyzes the impact on the landscape of drug research and development through a comprehensive analysis of newly approved anticancer drugs in China. The innovative drug development in China has greatly benefited from pro-innovation policies and expedited program designations. The number of imported and domestic new anticancer drugs has significantly increased, and the drug lag has been dramatically shortened.
Over the past two decades, China has introduced significant changes to drug regulations through regulatory innovations to accelerate drug review and approvals, keeping in line with the rapidly growing scientific innovation in drug research and development (R&D). In this study, we outlined the revolution of drug regulation in China since the establishment of the State Drug Administration in 1998. More particularly, we performed a comprehensive analysis of newly approved anticancer drugs in China from the year 2005 to May 2021, as a powerful illustration of how the revolution has changed the drug R&D landscape. Innovative drug development in China has boomed, benefiting in particular from pro-innovation policies as well as expedited program designations by the authority. We found a sig-nificant increase in the number of both imported and domestic new anticancer drugs from 2005 to 2021, with the emergence of drugs with novel mechanisms of action, including immune checkpoint inhibitors and cell therapy products. Drug lag has also been dramatically shortened by more than 70% for imported drugs in years 2016-2020 compared to years 2006-2010. Furthermore, we provide an insight into the potential approaches to further optimize the science-based and clinical value-based regulatory and R&D drug ecosystem in China. This review provides evidence of significant impacts of regulations and policies on drug R&D and suggests that the constantly adapting regulatory ecosystem will speed up drug devel-opment in China and worldwide.(c) 2022 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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