髓性白血病
阿扎胞苷
程序设计语言
医学
打开标签
开放标签研究
肿瘤科
儿科
内科学
计算机科学
不利影响
化学
DNA甲基化
程序设计语言
基因表达
基因
生物化学
作者
Olga Salamero,Antonieta Molero,Josè Antonio Pérez-Simón,Montserrat Arnán,Rosa Coll,Sara Garcia-Ávila,Evelyn Acuña‐Cruz,Isabel Cano,Tim C. P. Somervaille,S. Gutiérrez,María Isabel Arévalo,Jordi Xaus,Carlos Buesa,Ana Limón,Douglas V. Faller,Francesc Bosch,Pau Montesinos
标识
DOI:10.1016/s2352-3026(24)00132-7
摘要
Iadademstat is a potent, selective, oral inhibitor of both the enzymatic and scaffolding activities of the transcriptional repressor lysine-specific demethylase 1 (LSD1; also known as KDM1A) that showed promising early activity and safety in a phase 1 trial and strong preclinical synergy with azacitidine in acute myeloid leukaemia cell lines. Therefore, we aimed to investigate the combination of iadademstat and azacitidine for the treatment of adult patients with newly diagnosed acute myeloid leukaemia.
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