Tan Ruirong, Hua Hua, Zhou Siyuan, Yang Zhimin, Yang Changming, Huang Guo, Zeng Jin, Zhao Junning
Key Lab.: Biological Evaluation of TCM Quality of the State Administration of Traditional Chinese Medicine, Translational Chinese Medicine Key Laboratory of Sichuan Province, Sichuan Institute for Translational Chinese Medicine, Sichuan Academy of Chinese Medicine Sciences, Chengdu, China.
Center for Drug Evaluation, National Medical Products Administration (NMPA), Beijing, China.
Signal Transduct Target Ther. 2025 Jul 22;10(1):220. doi: 10.1038/s41392-025-02267-y.
The global pharmaceutical landscape remains dynamic and competitive, shaped by 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. Through this comparative analysis, the article underscores how China's evolving policy-driven innovation ecosystem has positioned it as a growing leader in global drug development. The review examines how enhanced regulatory efficiency, clinical trial progress, manufacturing capabilities, and international collaboration have bolstered China's growing influence, while also discussing the future opportunities and challenges it faces in shaping global pharmaceutical innovation and development.
全球制药格局依然充满活力且竞争激烈,受到一流疗法和突破性技术进步的影响。美国在一流疗法和突破性技术方面保持领先地位,这得益于先进的监管途径、跨国公司的大量投资、强大的研发人才队伍以及持续的技术创新。此外,美国食品药品监督管理局(FDA)通过“奥比斯计划”等合作进一步扩大了其全球影响力,该计划促进了全球多个监管机构对癌症治疗药物的同步审评。欧洲虽然历史上实力强劲,但在保持竞争优势方面面临着越来越大的挑战,特别是由于监管时间冗长以及成员国之间复杂的协调问题。在这种竞争激烈的全球环境下,中国已迅速从一个以仿制药为主的市场转变为创新药物研发的关键参与者。本文回顾了中国在2019年至2023年期间创新药物研发的进展,重点强调了监管现代化、临床试验进展以及新型疗法的出现。通过将中国的发展与上述全球同行进行比较,本综述突出了中国在监管效率、临床试验进展以及生物制品、细胞和基因疗法等创新疗法开发方面取得的成就。通过这种比较分析,本文强调了中国不断发展的政策驱动型创新生态系统如何使其在全球药物研发中日益成为领导者。该综述探讨了监管效率的提高、临床试验的进展、生产能力以及国际合作如何增强了中国日益增长的影响力,同时也讨论了中国在塑造全球制药创新与发展方面面临的未来机遇和挑战。