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Targeting kinases: A new approach to treating inflammatory rheumatic diseases

机译:靶向激酶:治疗炎性风湿病的新方法

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摘要

After two decades of research and development activity focussed on orally active kinase inhibitors, the first such drug (the JAK inhibitor Xeljanz, tofacitinib) was approved by the FDA in November 2012 for the treatment of rheumatoid arthritis (RA). There is an intense activity in many companies both on expanding the utility of JAK inhibitors in other auto-immune indications and in discovering inhibitors of the JAK family with different and more selective profiles. Progress is also being made with orally active Syk inhibitors. One such inhibitor (fostamatinib) is currently in large-scale phase 3 trials, and there are others in clinical development. The last two to three years have been transformative for kinase inhibitors in auto-immune diseases, as several inhibitors have finally progressed beyond phase 2 trials after so many failures on other targets. Thus, there are new treatment options for RA patients beyond existing oral DMARDs and parenteral biologics.
机译:在专注于口服活性激酶抑制剂的二十多年研发活动之后,第一种此类药物(JAK抑制剂Xeljanz,托法替尼)于2012年11月被FDA批准用于治疗类风湿关节炎(RA)。在许多公司中,在扩大JAK抑制剂在其他自身免疫适应症中的用途以及发现具有不同且更具选择性的特征的JAK家族抑制剂方面,都开展了激烈的活动。口服活性Syk抑制剂也正在取得进展。一种此类抑制剂(fostamatinib)目前正在大规模的3期试验中,还有其他还在临床开发中。在过去的两到三年中,自身免疫疾病中的激酶抑制剂发生了变革,因为在其他靶标上发生了许多失败之后,几种抑制剂终于超越了2期试验。因此,除了现有的口服DMARD和肠胃外生物制剂外,RA患者还有新的治疗选择。

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