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Anti-interleukin-23 agents for the treatment of ulcerative colitis

机译:用于治疗溃疡性结肠炎的抗白细胞介素-23剂

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摘要

Introduction: Treatment of ulcerative colitis (UC) aims to control symptoms and to suppress intestinal inflammation. Despite considerable advances, a proportion of patients do not respond to currently available drugs. The interleukin (IL)-23 axis plays a significant role in the pathogenesis of UC and has thus become an important target for drug development. Areas covered: The review briefly summarizes the pathophysiology of the IL-12/23 axis and provides a synopsis of the available evidence for efficacy and safety of ustekinumab, mirikizumab (LY3074828), risankizumab (BI655066/ABBV066), brazikumab (MEDI2070; formerly AMG139) and guselkumab (CNTO1959) in UC. We also provide an overview of ongoing and anticipated trials in this field. Expert opinion: A Phase 2 trial with mirikizumab and a Phase 3 trial with ustekinumab have demonstrated the efficacy of anti-IL-23 agents in achieving clinical and endoscopic outcomes in UC with a favorable safety profile. Trials of other anti-IL-23 agents in UC are under way and designed to explore head-to-head efficacy with existing biologics, as well as the prospect of combination biological therapy. Apart from data on longer term efficacy and safety, future trials should also explore strategies to inform the positioning of IL-23 antagonists in therapeutic algorithms.
机译:介绍:溃疡性结肠炎(UC)的治疗旨在控制症状并抑制肠炎症。尽管进展相当大,但一部分患者不响应目前可用的药物。白细胞介素(IL)-23轴在UC的发病机制中起着重要作用,因此成为药物发育的重要目标。所涵盖的区域:审查简要介绍了IL-12/23轴的病理生理学,并提供了Ustekinumab,Mirikizumab(Ly3074828),Risankizumab(Bi655066 / Abv066),Brazikumab(Medi2070;以前的AMG139)的有效性和安全性的可用证据UC中的Guselkumab(CNTO1959)。我们还概述了该领域的持续和预期的试验。专家意见:使用Mirikizumab的第2阶段试验和Ustekinumab的第3阶段试验表明,抗IL-23药剂在具有有利安全性型材的UC中实现临床和内窥镜结果的疗效。在UC中的其他抗IL-23代理商的试验并旨在探讨现有的生物制剂的头脑效果,以及组合生物治疗的前景。除了较长术语疗效和安全性的数据外,未来的试验还应探索策略,以告知IL-23拮抗剂在治疗算法中的定位。

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