後者是目前la/mUC的一線標準療法。3月28日,安斯泰來光光算谷歌seo算谷歌seo代运营製藥集團宣布,中國國家藥品監督管理局(NMPA)藥品審評中心(CDE)已於2024年3月27日受理enfortumab vedotin與pembrolizumab(帕博利珠單抗)聯合用藥用於一線治療既往未經治療的局部晚期或轉移性尿路上皮癌(la/mUC)成年患者的補充生物製劑許可申請(sBLA)。enfortumab 光算谷歌seove光算谷歌seo代运营dotin與pembrolizumab聯合用藥有可能改變現有的治療模式 ,如獲批,成為首個光算谷光算谷歌seo歌seo代运营替代含鉑化療的聯合療法,(文章來源:界麵新聞) |
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