亚洲的细胞和基因疗法批准:监管格局,获取和负担能力
William Ying Khee Hwang1, Sudipto Bari2, Shin Kawamata3
1National Cancer Centre Singapore, Singapore, Singapore; Singapore General Hospital, Singapore, Singapore.
Cytotherapy
|September 28, 2025
概括
细胞和基因疗法 (CGTs) 为罕见疾病提供治愈潜力. 本综述分析了亚洲六个市场的CGT监管框架,定价和退款,突出了在获取和负担能力方面取得的进展和持续的挑战.
科学领域:
- 生物技术是生物技术.
- 卫生政策 卫生政策
- 药物经济学 药物经济学
背景情况:
- 细胞和基因疗法 (CGTs) 代表了治疗罕见和危及生命的疾病的变革性方法.
- 亚洲CGT市场已出现显著增长,受监管进步和产品审批增加的推动.
研究的目的:
- 为新加坡,日本,韩国,中国,印度和泰国提供CGT监管框架,产品批准,定价和退款的全面分析.
- 检查在这些关键亚洲市场的监管成熟度,准入,负担能力和制造能力的差异.
- 确定亚洲CGT行业的协调,公平获取和未来政策规划的机会.
主要方法:
- 对2023年至2025年更新数据的比较分析.
- 审查监管框架,产品批准,定价趋势和退款政策.
- 检查当地制造能力和创新驱动因素.
主要成果:
- 日本和韩国已经为CGT实施了快速监管途径.
- 印度和中国正在强调国内创新,以降低CGT成本.
- 持续面临的挑战包括该地区的可负担性,可扩展性和可持续的报销模式.
结论:
- 亚洲的CGT景观正在迅速发展,具有多样化的监管方法和不同程度的市场准入.
- 解决负担能力和报销方面的挑战对于确保公平获得CGT至关重要.
- 政策协调和持续创新是亚洲CGT行业未来增长和可持续性的关键.
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