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2018-2024年中国干细胞药物IND申请受理数量(例)
2018-2024年中国干细胞药物IND申请受理数量(例)
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图片大小:79KB
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所属报告:
中源协和-公司研究报告-立足“精准医疗”全产业链抢滩干细胞创新药产业化发展空间-241222(26页).pdf
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IND批准数量:国产新药主导,占比持续提升
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行业数据
2026-06-11
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2020-2025中国IND申报受理及获批数量(个)
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行业数据
2026-05-25
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美国FDA药物评价与研究中心受理的IND申请
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行业数据
2026-04-08
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中国NMPA药品审评中心受理的IND申请
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行业数据
2026-04-08
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图11国内IND获批数量和已启动临床I期研究数量情况
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行业数据
2026-03-10
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表 3-2 间充质干细胞获批药物(2011年—2025年)
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行业数据
2026-03-03
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一建立了干细胞规模化扩增技术,解决干细胞数量问题
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市场规模
2026-03-03
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图40、2020-2025年中国创新药IND和NDA年
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行业数据
2026-02-28
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图41、2020Q1-2025Q4年中国创新药IND和
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行业数据
2026-02-28
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黄色表示2025年IND申报数量达到新高
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行业数据
2026-02-04
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2025年11月创新药的NDA、IND申请(首次申请)
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行业数据
2025-12-26
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图表4中国IND的数量、增速和趋势
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行业数据
2025-12-01
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2025年10月创新药的NDA、IND申请(首次申请)
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行业数据
2025-11-13
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人类多能干细胞分化为多巴胺能神经元
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行业数据
2025-09-16
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神经干细胞(hNSC)帕金森治疗生物学原理
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行业数据
2025-09-16
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两个阶段,以确保其安全性、有效性和质量可控性;第二种为医疗技术监管路径,医疗机构或研究者在开展干细胞临床研究前,需要向卫健委申请机构/项目备案,并遵循相关的医疗技术管理规定。随着政府对干细胞等细胞治疗产业认识的持续加深,从顶层设计到地方法规,多个政策文件明确支持干细胞创新药物的发展,继续加强干细胞技术的监管和执法力度,推动干细胞技术的标准化和规范化发展。据前瞻产业研究院数据,我国干细胞药物IND申请受理量近年来快速提升,2023年已达52例,远高于2018年的5例。
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中源协和-公司研究报告-立足“精准医疗”全产业链抢滩干细胞创新药产业化发展空间-241222(26页).pdf
2018-2024年中国干细胞药物IND申请受理数量(例)
2011-2023年我国60岁以上人口及占总人口比重
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