阿斯利康旗下Koselugo获美国FDA批准用于成人Ⅰ型神经纤维瘤病治疗

环球市场播报11-21

阿斯利康公司周四宣布，美国食品药品监督管理局已批准口服MEK抑制剂Koselugo （selumetinib）用于治疗有症状、无法手术切除的丛状神经纤维瘤（PN）的成人神经纤维瘤病1型（NF1）患者。该批准基于KOMET III期临床试验结果，该试验显示成人患者中肿瘤大小减少的总体响应率为20%。海量资讯、精准解读，尽在新浪财经APP 责任编辑：张俊 SF065

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