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康宁杰瑞制药-B：JSKN022 IND申请获CDE正式受理_蜘蛛资讯网

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公告，公司自主研发的程序性死亡配体1（PD-L1）/ 整合素αvβ6双特异性抗体偶联药物（ADC）JSKN022新药临床试验（IND）申请，已获中国国家药品监督管理局（NMPA）药品审评中心（CDE）正式受理。本公司计划开展用于治疗晚期恶性实体瘤的JSKN022首次人体临床研究。　　目前全球范围内尚无靶向整合素αvβ6或PD-L1的ADC上市，相关在研药物均处于临床研究阶段。临床前数据显示，JSK

，对整合素αvβ6 和/或PD-L1表达阳性的肿瘤细胞具有抗肿瘤活性，有望为PD-1/PD-L1抑制剂耐药或治疗无效的肿瘤（如非小细胞肺癌、头颈部鳞状细胞癌、结直肠癌等）患者提供新的治疗选择。责任编辑：卢昱君

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