Etrasimod: revisión de la seguridad y las consideraciones prácticas de manejo de una nueva terapia oral para el tratamiento de la colitis ulcerosa

IF 1.9 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY
Gastroenterologia y hepatologia Pub Date : 2026-05-01 Epub Date: 2025-12-20 DOI:10.1016/j.gastrohep.2025.502647
Yamile Zabana , Ana Cábez , Ana Gutiérrez Casbas
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引用次数: 0

Abstract

Modulation of sphingosine-1-phosphate receptors represents a relatively recent approach in the treatment of inflammatory bowel disease, although these modulators have been approved since 2010 for other inflammatory conditions such as multiple sclerosis. Etrasimod is a sphingosine-1-phosphate receptor (S1PR) modulator that binds to S1PR1, S1PR4 and S1PR5 receptors, and its efficacy has been demonstrated in the treatment of moderately to severely active ulcerative colitis. It is a small molecule and synthetic drug administered orally, with a proper bioavailability and a fast elimination rate, predictable pharmacokinetics and lack of immunogenicity, which are convenient characteristics for both efficacy and safety. This article reviews the pharmacological characteristics of etrasimod and its safety profile.
伊特拉西莫德:一种治疗溃疡性结肠炎的新型口服疗法的安全性和实际管理考虑的综述。
鞘氨醇-1-磷酸(S1P)受体的调节是治疗炎症性肠病的一种相对较新的方法,尽管S1P调节剂自2010年以来已被批准用于其他炎症性疾病,如多发性硬化症。Etrasimod是一种S1P受体(S1PR)调节剂,可结合S1PR1、S1PR4和S1PR5受体,其疗效已被证明可治疗中度至重度活动性溃疡性结肠炎。它是一种口服小分子合成药物,具有生物利用度合适、消除速度快、药代动力学可预测、缺乏免疫原性等特点,既有效又安全。本文综述了伊特拉西莫德的药理学特性及其安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Gastroenterologia y hepatologia
Gastroenterologia y hepatologia GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
1.50
自引率
10.50%
发文量
147
审稿时长
48 days
期刊介绍: Gastroenterology and Hepatology is the first journal to cover the latest advances in pathology of the gastrointestinal tract, liver, pancreas, and bile ducts, making it an indispensable tool for gastroenterologists, hepatologists, internists and general practitioners.
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