Department of Cellular and Molecular Biology, Scripps Research, La Jolla, CA, United States.
Department of Chemistry, Scripps Research, La Jolla, CA, United States.
Adv Pharmacol. 2024;101:183-202. doi: 10.1016/bs.apha.2024.10.003. Epub 2024 Oct 16.
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.
鞘氨醇-1 磷酸(S1P)调节剂最近获得了美国食品和药物管理局(FDA)的批准,用于治疗中重度溃疡性结肠炎,包括 2021 年批准的奥扎尼莫德和 2023 年批准的埃特拉莫德。这些口服药物在 UC 中具有独特的疗效,因为它们具有多种机制,有助于其有益的免疫调节作用,同时保留宿主对病原体的反应,并减轻与非特异性药物相关的毒性。在这篇综述中,详细描述了第一个批准的 S1P 调节剂奥扎尼莫德的发现和开发:从最初的筛选设计到发现独特的结合剂,再到广泛的化学修饰以改善药代动力学和安全性特征,以及通过临床前和临床研究验证机制和建立安全性和疗效。最终,这篇综述不仅将使读者了解用于 UC 的临床 S1P 调节剂的独特开发途径,还将突出强调为炎症性肠病个体化治疗方法所取得的进展和仍存在的差距。