关于中国孤儿药研发的专利分析观点:现状和技术特征
Yang Jiao1, Fangzhe Yuan1, Tianyu Liu1
1School of International Business Pharmaceutical, China Pharmaceutical University, Nanjing, China.
Therapeutic innovation & regulatory science
|February 16, 2026
概括
中国中国中国中国.
科学领域:
- 制药科学 制药科学
- 生物技术是生物技术.
- 公共卫生政策 公共卫生政策
背景情况:
- 罕见疾病对全球健康构成重大挑战,需要国际合作.
- 分析了中国的孤儿药物创新格局,以了解研发 (R&D) 趋势并为政策提供信息.
- 从1995年到2023年的专利数据被用来绘制中国孤儿药研发的演变图.
研究的目的:
- 分析中国的孤儿药物的专利申请.
- 确定研发模式,关键治疗领域和主导技术.
- 探索解决罕见病未满足需求的政策影响.
主要方法:
- 分析了来自中国实体的323份专利合作条约申请 (1995-2023年).
- 利用国际专利分类 (IPC) 和双边网络建模.
- 将疾病映射到中国罕见病目录,并使用网络指标量化疾病技术联系.
主要成果:
- 专利申请在2018-2023年期间增加了58.2% (188项专利),与监管改革保持一致.
- 创新集中在瘤学和神经学领域,其中66.2%的罕见疾病缺乏专利覆盖.
- 主要技术包括小分子和基因疗法;与美国合作伙伴关系存在协作研发生态系统.
结论:
- 中国的孤儿药物创新正在增长,但在疾病和技术上分布不均.
- 政策干预,包括分层激励和专门资金,对于被忽视的罕见疾病至关重要.
- 全球伙伴关系对于促进公平获得罕见疾病治疗是必不可少的.
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