Wang Qiwei, Ling Xing, Dai Zhengli, Wang Xiaoling, Guo Wen, Chen Guiliang
China State Institute of Pharmaceutical Industry, Shanghai, China.
China Pharmaceutical Industry Information Center, Shanghai, China.
Front Pharmacol. 2025 Mar 26;16:1561095. doi: 10.3389/fphar.2025.1561095. eCollection 2025.
The accessibility of pediatric medicine is a global challenge. The issuance of the "Several Opinions on Ensuring the Use of Children's Medicine" by six ministries in China in 2014 marked the formation of the policy framework. This study aims to systematically review the progress and achievements of incentive policies for China's pediatric medicine.
By analyzing policy documents, clinical trial data, review and approval results, medical insurance directories, volume-based procurement data, as well as adverse reaction reports, the implementation effects of incentive policies for China's pediatric medicine were assessed.
China has made progress in legislation, research and development, review and approval, production, access, payment, and use of pediatric medicine. The number and variety of pediatric clinical trials have increased year by year. Some medicine on the Encouraged Research and Submission List of Pediatric Medicine have successfully entered the market. Priority review and approval policies have effectively facilitated the rapid approval of pediatric medicine. However, the availability still needs to be improved, especially in the field of medicine for young children (<6 years).
Although incentive policies for China's pediatric medicine have achieved favorable effects, the synergy of the policies still needs to be strengthened. It is recommended that the Chinese government place greater emphasis on the introduction of mandatory regulations and incentive policies, enhance the synergy between policies, use a combination of fiscal and medical insurance tools and follow up on the application of new technologies to comprehensively improve the accessibility of pediatric medicine in the future. This might be helpful for guaranteeing the safety, efficacy and economy of pediatric medicine.
儿科用药的可及性是一项全球性挑战。2014年中国六部委发布《关于保障儿童用药的若干意见》,标志着政策框架的形成。本研究旨在系统回顾中国儿科用药激励政策的进展与成效。
通过分析政策文件、临床试验数据、审评审批结果、医保目录、带量采购数据以及不良反应报告,评估中国儿科用药激励政策的实施效果。
中国在儿科用药的立法、研发、审评审批、生产、可及性、支付和使用等方面均取得了进展。儿科临床试验的数量和品种逐年增加。一些儿科用药鼓励研发申报清单上的药品已成功上市。优先审评审批政策有效促进了儿科用药的快速获批。然而,可及性仍有待提高,尤其是在幼儿(<6岁)用药领域。
尽管中国儿科用药激励政策取得了良好效果,但政策协同效应仍需加强。建议中国政府更加重视出台强制性法规和激励政策,增强政策之间的协同效应,综合运用财政和医保工具,并跟踪新技术应用,以全面提高未来儿科用药的可及性。这可能有助于保障儿科用药的安全性、有效性和经济性。