拜耳(BAYRY.US)宣佈Sevabertinib獲FDA優先審評用於治療HER2突變NSCLC

智通財經

05-29

智通財經APP獲悉，5月28日，拜耳(BAYRY.US)宣佈Sevabertinib(BAY 2927088)獲FDA授予優先審評資格，用於治療已經接受過一種系統治療的HER2突變非小細胞肺癌患者。

Sevabertinib爲拜耳的核心管線之一，此前已經獲得中國、美國的突破療法認證，目前正在推進三期驗證性臨牀SOHO-02，以及HER2激活突變泛瘤種的二期臨牀panSOHO。

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