【阿斯利康PD-L1肿瘤药在中国获批第四项适应证】金十数据3月10日讯，阿斯利康中国宣布，度伐利尤单抗注射液（商品名：英飞凡）近日获得中国国家药品监督管理局(NMPA)正式批准，联合含铂化疗作为新辅助治疗，术后继续以本品作为单药辅助治疗，用于治疗可手术切除的Ⅱ、ⅢA和ⅢB期且无已知表皮生长因子受体（EGFR）突变或间变性淋巴瘤激酶（ALK）重排的成人非小细胞肺癌（NSCLC）患者。度伐利尤单抗是一种人源化的PD-L1单克隆抗体，是阿斯利康旗下明星抗癌药，2024年全球收入47.17亿美元，同比增长21%。此次是度伐利尤单抗在中国获批的第4项适应证。
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