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面肩肱型肌营养不良症(FSHD):Losmapimod的I期临床试验取得积极结果

2019-10-05 Allan MedSci原创

面肩肱型肌营养不良症(FSHD)是一种遗传性肌肉疾病,受其影响最严重的是脸、肩、上臂等部位的肌肉,该疾病是由骨骼肌细胞中DUX4的错误表达引起的。

面肩肱型肌营养不良症(FSHD)是一种遗传性肌肉疾病,受其影响最严重的是脸、肩、上臂等部位的肌肉,该疾病是由骨骼肌细胞中DUX4的错误表达引起的。专注于罕见疾病治疗的临床阶段生物制药公司Fulcrum近日宣布,选择性p38α/β丝裂原活化蛋白激酶(MAPK)抑制剂Losmapimod能够降低FSHD患者肌肉细胞中DUX4基因的表达。这项I期临床试验结果由Fulcrum Therapeutics的医学总监Michelle Mellion医师在丹麦哥本哈根举行的第24届世界肌肉协会国际年会上进行了口头报告。

Michelle Mellion医师表示:“Losmapimod在FSHD患者的I期临床试验中得出的初步结果表明,Losmapimod具有良好的耐受性,并在血浆和肌肉中达到了剂量依赖性浓度,根据临床前药理学研究认为该药物足以达到预期疗效”。


原始出处:

http://www.firstwordpharma.com/node/1671733#axzz61Rlned4y

本文系梅斯医学(MedSci)原创编译整理,转载需授权!


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    2019-10-07 江川靖瑶
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    2019-10-05 坚强007

    向科研人员致敬!!!

    0

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p38丝裂原活化蛋白激酶(MAPK)刺激炎症参与动脉粥样硬化的形成,还与斑块不稳定和心肌梗死(MI)的过程有关。非ST段抬高MI的2期临床试验数据表明,p38 MAPK抑制剂losmapimod可减轻炎症、提高疗效。因此研究者进行了一项随机、安慰剂对照、双盲研究(LATITUDE-TIMI 60),探究losmapimod对急性MI住院患者的安全性和有效性。研究纳入了2013-6-3至2015-1

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