提高儿科对细胞和基因疗法的准入
Crystal L Mackall1,2,3, Catherine M Bollard4, Nancy Goodman5
1Center for Cancer Cell Therapy, Stanford Cancer Institute, Stanford University School of Medicine, Stanford, CA, USA. cmackall@stanford.edu.
Nature medicine
|June 17, 2024
概括
由于成本高昂,细胞和基因疗法 (CGTs) 在儿科疾病中面临市场失败. 一种新的儿科先进药物生物技术可以克服这一问题,改善儿童获得重要治疗的机会.
科学领域:
- 生物技术是生物技术.
- 儿科医学 儿科医学
- 药物开发 药物开发
背景情况:
- 细胞和基因疗法 (CGTs) 对儿科疾病有希望.
- 传统的生物制药模型在小儿市场规模方面扎,导致市场失败.
- 高昂的制造成本,监管障碍和不一致的许可做法阻碍了儿科CGT的发展.
研究的目的:
- 确定导致儿科CGT市场失败的关键因素.
- 提出一种新的解决方案,以解决儿科CGT的开发和商业化差距.
- 提高儿童获得拯救生命的CGT治疗的机会.
主要方法:
- 对当前生物制药开发模型的前景分析.
- 确定儿科CGT开发和商业化方面的挑战.
- 关于新组织结构的建议:儿科先进药物生物技术.
主要成果:
- 传统模式对儿科CGT发展构成重大障碍.
- 一个新的实体可以弥合儿科CGT的"死亡之谷".
- 学术界,制造业和监管机构之间的合作至关重要.
结论:
- 一个专门的实体,儿科先进药物生物技术,被提议克服市场失败.
- 这一实体将促进传统模式之外的后期开发和商业化.
- 该倡议旨在增加美国儿科患者获得创新的CGT的机会.
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