拜耳(BAYRY.US)宣布Sevabertinib获FDA优先审评用于治疗HER2突变NSCLC

智通财经

05-29

智通财经APP获悉，5月28日，拜耳(BAYRY.US)宣布Sevabertinib(BAY 2927088)获FDA授予优先审评资格，用于治疗已经接受过一种系统治疗的HER2突变非小细胞肺癌患者。

Sevabertinib为拜耳的核心管线之一，此前已经获得中国、美国的突破疗法认证，目前正在推进三期验证性临床SOHO-02，以及HER2激活突变泛瘤种的二期临床panSOHO。

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