发现和开发治疗溃疡性结肠炎的 1-磷酸鞘氨醇受体调节剂 ozanimod。

Q1 Pharmacology, Toxicology and Pharmaceutics
Advances in pharmacology Pub Date : 2024-01-01 Epub Date: 2024-10-16 DOI:10.1016/bs.apha.2024.10.003
Hugh Rosen, Edward Roberts
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引用次数: 0

摘要

磷酸鞘氨醇-1(S1P)调节剂最近获得了美国食品及药物管理局(FDA)的批准,用于治疗中度至重度溃疡性结肠炎,其中包括 2021 年批准的药物奥扎莫德(ozanimod)和 2023 年批准的药物艾曲昔莫德(etrasimod)。这些口服药物对溃疡性结肠炎具有独特的疗效,因为它们具有多模式机制,有助于产生有益的免疫调节效应,同时保持宿主对病原体的反应,并减轻特异性较低的药物的毒性。本综述详细介绍了首个获批的 S1P 调节剂奥扎莫德的发现和开发过程:从设计初始筛选以发现独特的结合剂,到进行广泛的化学修饰以改善药代动力学和安全性,再到进行临床前和临床研究以验证机制并确定安全性和有效性。最终,这篇综述不仅会让读者了解临床 S1P 调制剂治疗 UC 的独特开发路径,而且还会强调在炎症性肠病个体化治疗方法方面取得的进展和尚存的差距。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The discovery and development of the sphingosine 1-phosphate receptor modulator ozanimod in ulcerative colitis.

Sphingosine-1 phosphate (S1P) modulators have received recent FDA-approval for the treatment of moderate-to-severe ulcerative colitis, including agents ozanimod, approved in 2021, and etrasimod, approved in 2023. These oral drugs are uniquely efficacious in UC as they have multimodal mechanisms contributing to their beneficial immunomodulatory effects, while preserving host response to pathogens and attenuating toxicities observed with less specific agents. In this review, the discovery and development of the first approved S1P modulator, ozanimod, is described in detail: from design of initial screens to discover unique binding agents, to extensive chemical modifications to improve pharmacokinetic and safety profiles, and through preclinical and clinical studies validating mechanism and establishing safety and efficacy. Ultimately, this review will not only inform the reader of the unique path to development of a clinical S1P modulator for UC, but will also highlight advances made and gaps remaining to individualize therapeutic approaches for inflammatory bowel disease.

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来源期刊
Advances in pharmacology
Advances in pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
9.10
自引率
0.00%
发文量
45
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