Menin-MLL抑制剂KO-539获FDA的孤儿药物认定用于治疗急性髓细胞白血病

2019-07-25 Allan MedSci原创

Kura Oncology是一家临床阶段的生物制药公司,专注于开发用于治疗肿瘤的精准药物,近日宣布美国食品和药品监督管理局(FDA)已授予Menin-MLL抑制剂KO-539孤儿药物认定,用于治疗急性髓性白血病(AML)。

Kura Oncology是一家临床阶段的生物制药公司,专注于开发用于治疗肿瘤的精准药物,近日宣布美国食品和药品监督管理局(FDA)已授予Menin-MLL抑制剂KO-539孤儿药物认定,用于治疗急性髓性白血病AML)。

Kura Oncology总裁兼首席执行官Troy Wilson博士说:“AML的孤儿药物指定代表了KO-539发展的一个重要里程碑。FDA并认识到KO-539有可能解决AML患者的高度未满足的医疗需求。我们的临床前数据也是令人鼓舞的


原始出处:

http://www.firstwordpharma.com/node/1654850#axzz5ug3cIKrI

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    2020-01-10 s_pl2008
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    2020-03-02 tastas
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    2019-12-22 jklm09
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    2019-07-27 chengjn
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