奥扎莫德治疗溃疡性结肠炎的最新进展。

IF 1.8 4区 医学 Q2 Medicine
Elisabetta K Antonelli, Rachele Del Sordo, Olivia Morelli, Vincenzo Villanacci, Gabrio Bassotti
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引用次数: 0

摘要

治疗中度至重度溃疡性结肠炎(UC)已经丰富了越来越多的药物可用于这种疾病。然而,在许多UC患者中,常规治疗失败,反应不完全或对生物制剂的反应丧失。因此,在UC的治疗武器库中,对新药的需求仍在增长。Ozanimod是一种鞘氨醇-1-磷酸(S1P)受体调节剂,最近被批准用于UC治疗。本文就盐酸ozanimod在肠道炎症的临床前研究中的作用机制,以及其在中重度UC患者中的临床有效性和安全性进行综述。在这一人群中,ozanimod在诱导临床缓解方面明显比安慰剂更有效。此外,在临床反应、无皮质类固醇缓解、内镜改善和粘膜愈合方面,ozanimod在该人群中的表现明显优于安慰剂。在UC的临床试验中没有出现ozanimod明显的安全性问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Update on ozanimod for ulcerative colitis.

Treating moderate to severe ulcerative colitis (UC) has been enriched by the increasing number of drugs available for this disease. However, failure of conventional therapies, an incomplete response, or loss of response to biologics is experienced in many UC patients. Thus, there is still a growing need for new drugs in the therapeutic arsenal for UC. Ozanimod is a sphingosine-1-phosphate (S1P) receptor modulator which has been recently approved for UC therapy. In this review, we focus on the mechanism of action of ozanimod hydrochloride in preclinical studies of intestinal inflammation as well as its clinical effectiveness and safety in moderate to severe UC patients. In this population, ozanimod was shown to be significantly more effective than placebo to induce clinical remission. Additionally, in terms of clinical response, corticosteroid-free remission, endoscopic improvement and mucosal healing, ozanimod performed significantly better than placebo in this population. No significant safety concerns about ozanimod emerged from clinical trials in UC.

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来源期刊
Drugs of today
Drugs of today 医学-药学
CiteScore
3.90
自引率
0.00%
发文量
48
审稿时长
6-12 weeks
期刊介绍: An international, peer-reviewed journal publishing monographs on new products entering the market and review articles. Since its inception in 1965, Drugs of Today has established a reputation for excellence in providing physicians and other key healthcare professionals with practical, up-to-date monographs on recently approved and launched drugs.
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