欧洲药品管理局人用医药产品委员会（CHMP）近日发布积极意见，建议授予安进公司开发的靶向疗法Imdylltra（Tarlatamab）上市许可。该药物拟用于治疗既往接受过系统性治疗的复发广泛期小细胞肺癌患者。
此次推荐基于关键临床研究数据，显示Tarlatamab作为双特异性T细胞衔接抗体，能显著激活患者自身免疫系统攻击肿瘤细胞。若最终获欧盟委员会批准，这将成为首款针对该适应症的靶向免疫疗法，为预后极差的晚期肺癌群体提供新的治疗选择。
欧洲药品管理局人用医药产品委员会（CHMP）近日发布积极意见，建议授予安进公司开发的靶向疗法Imdylltra（Tarlatamab）上市许可。该药物拟用于治疗既往接受过系统性治疗的复发广泛期小细胞肺癌患者。
此次推荐基于关键临床研究数据，显示Tarlatamab作为双特异性T细胞衔接抗体，能显著激活患者自身免疫系统攻击肿瘤细胞。若最终获欧盟委员会批准，这将成为首款针对该适应症的靶向免疫疗法，为预后极差的晚期肺癌群体提供新的治疗选择。
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