FDA批准阿替利珠单抗用于部分患者肌层浸润性膀胱癌的辅助治疗

投资观察05-16 00:58

美国食品药品监督管理局(FDA)已批准阿替利珠单抗用于存在分子残留病灶的肌层浸润性膀胱癌患者的辅助治疗。

同时，FDA亦批准将Natera公司的Signatera CDX作为泰圣奇膀胱癌治疗的伴随诊断工具，适用于部分患者。

（注：文中提及的公司代码为ROPC.S）

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