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首页> 外文期刊>Drugs of the Future >Vobarilizumab Anti-interleukin-6 receptor subunit alpha (CD126; IL-6R) Treatment of rheumatoid arthritis Treatment of systemic lupus erythematosus
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Vobarilizumab Anti-interleukin-6 receptor subunit alpha (CD126; IL-6R) Treatment of rheumatoid arthritis Treatment of systemic lupus erythematosus

机译:Vobarilizumab抗白细胞介素-6受体亚基α(CD126; IL-6R)治疗风湿性关节炎的系统性狼疮性血红肿

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摘要

The development of monoclonal antibodies targeting proinflammatory mediators has revolutionized treatment for patients with rheumatoid arthritis who have failed to show an adequate clinical response to disease-modifying antirheumatic drugs. However, a significant number of patients continue to show unacceptable levels of disease activity. Tocilizumab and sarilumab, both anti-interleukin-6 receptor (IL-6R) antibodies, have great efficacy in such patients, but have been associated with some unwanted side effects. The European League Against Rheumatism and American College of Rheumatology consensus is that new treatments should induce and maintain remission, while minimizing side effects. Vobarilizumab (ALX-0061) is a bispecific Nanobody that targets IL-6R and human serum albumin. The latter of which significantly extends its serum half-life. Both tocilizumab and vobarilizumab target the soluble and membrane-bound forms of the receptor, but vobarilizumab has much greater affinity for the soluble receptor, which is believed to be associated with the proinflammatory action of IL-6. In phase II clinical trials, both drugs showed similar efficacy but vobarilizumab use was associated with fewer adverse events. Vobarilizumab reduced disease activity scores and induced lasting remission and is expected to enter phase III trials in the near future.
机译:靶向促炎介质的单克隆抗体的发展对类风湿性关节炎的患者进行了彻底改变治疗,该患者未能表现出对疾病改性的抗抗肠药物的充分临床反应。然而,大量患者继续表现出不可接受的疾病活动水平。 Tocilizumab和Sarilumab,抗白细胞介素-6受体(IL-6R)抗体,在这些患者中具有很大的疗效,但已经与一些不需要的副作用有关。欧洲联盟对风湿病和美国风湿病学院共识是,新的治疗应该诱导和维持缓解,同时最大限度地减少副作用。 vobarilizumab(Alx-0061)是靶向IL-6R和人血清白蛋白的双特异性纳米型。后者显着延伸了其血清半衰期。 Tocolizumab和vobarilizumab靶向受体的可溶性和膜结合形式,但Vobarilizumab对可溶性受体具有更大的亲和力,其被认为与IL-6的促炎作用相关。在II期临床试验中,两种药物表现出类似的疗效,但触发物使用与更少的不良事件有关。川芎降低疾病活动分数并引起持久的缓解,预计将在不久的将来进入第三阶段试验。

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