南方财经4月25日电,辉瑞公司今日宣布,其口服靶向药英立达?(Inlyta?,通用名:阿昔替尼片)于2025年4月22日获得国家药品监督管理局(NMPA)批准,联合特瑞普利单抗用于中高危的不可切除或转移性肾细胞癌(RCC)患者的一线治疗,这也是中国肾癌治疗领域首个且唯一获批的一线靶免联合治疗方案。(21世纪经济报道)
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