信达生物:IBI363获国家药监局纳入突破性治疗药物品种,治疗晚期黑色素瘤

每日经济新闻
31 Mar

每经AI快讯,据信达生物官微消息,3月31日,信达生物制药集团宣布,其全球首创PD-1/IL-2α-bias双特异性抗体融合蛋白IBI363已被中国国家药品监督管理局(NMPA)药品审评中心(CDE)纳入突破性治疗药物(BTD)品种名单,拟定适应症为既往未经过系统性治疗的不可切除局部晚期或转移性肢端型及黏膜型黑色素瘤。(文章来源:每日经济新闻)

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