中国儿科药物开发:现状和未来前景
Lin Song1, Ni Zhang2, Ting-Ting Jiang2
1Department of Pharmacy, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, China International Science and Technology Cooperation base of Child development and Critical Disorders, Children's Hospital of Chongqing Medical University, Chongqing, 400014, China.
Paediatric drugs
|June 5, 2024
概括
中国已经实施了许多政策,以推进儿科药物开发,导致在2018-2022年期间批准了172种儿科药物. 进一步的倡议鼓励研究和开发专门的儿童药物.
科学领域:
- 儿科药理学 儿科药理学
- 监管科学 监管科学
- 药物开发 药物开发
背景情况:
- 全球监管机构长期以来一直通过指导方针和法律促进儿科药物开发.
- 中国在2014年发布了关键政策和随后的法规,以优先考虑和支持儿科药物开发.
- 取得了重大进展,从2018年到2022年批准了172种儿科药物.
研究的目的:
- 分析促进中国儿科药物开发的法规.
- 审查中国儿科药物批准,临床试验和标签的进展情况.
- 讨论中国儿科药物研发的当前挑战和未来战略.
主要方法:
- 分析法规,包括优先审查和批准系统,技术指南,数据保护和财务支持.
- 对儿科药物批准和临床试验数据的一般概况的审查.
- 检查销售药品标签更新,包括儿科信息.
主要成果:
- 在2018年至2022年期间,批准了172种专用儿科药物.
- 自2016年以来,已发布了四个儿科药物清单,包括129种药物.
- 大约有25种列出的药物已经获得批准,涵盖了瘤学,神经学和罕见疾病等领域.
结论:
- 中国已经建立了一个全面的监管框架,以促进儿科药物开发.
- 实施的政策导致批准的儿科药物显著增加.
- 应对现有的挑战对于中国儿科药物研发的持续进步至关重要.
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