和黄医药与信达生物联合宣布：爱优特®（呋喹替尼）联合达伯舒®（信迪利单抗注射液）获NMPA批准用于治疗局部晚期或转移性肾细胞癌_老虎社区_美港股上老虎

和黄医药与信达生物联合宣布：爱优特®（呋喹替尼）联合达伯舒®（信迪利单抗注射液）获NMPA批准用于治疗局部晚期或转移性肾细胞癌

美股速递05-21

和黄医药与信达生物今日共同发布公告，宣布其合作开发的联合疗法——爱优特®（呋喹替尼）与达伯舒®（信迪利单抗注射液）——已正式获得中国国家药品监督管理局的上市批准。该联合疗法获批用于治疗局部晚期或转移性肾细胞癌患者，为这一领域的临床治疗提供了新的重要选择。

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