揭开瑞替尼的神秘面纱:深入分析用于治疗斑秃的 JAK3 抑制剂。

IF 3.9 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Expert Opinion on Drug Metabolism & Toxicology Pub Date : 2024-09-09 DOI:10.1080/17425255.2024.2401603
Mariela Nunez,Supratik Kar,Katherine A Rodriguez,Dariel Ondieki
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引用次数: 0

摘要

简介:脱发(AA)是由于JAK/STAT通路失调导致的非瘢痕性脱发,长期以来一直缺乏有效的治疗方法。2023 年,新型 Janus 激酶 (JAK) 3 和酪氨酸激酶家族抑制剂 Ritlecitinib 首次获得美国 FDA 批准用于治疗 AA,随后日本、欧洲、中国和英国也相继批准了该药物。本综述概述了利特西替尼的药理特性、生物靶点和开发策略。它研究了该药的作用机制、药代动力学、药效学和临床试验见解。此外,它还涵盖了该药物的化学合成、禁忌症、药物相互作用和潜在不良反应,并特别关注了该药物在青少年、孕妇和老年人中的使用。虽然还需要长期的安全性数据和实际疗效研究,但它在成人和青少年中的口服给药和疗效使其成为一种潜在的变革性疗法。正在进行的研究应侧重于优化治疗策略、确定预测性生物标志物和评估成本效益,以充分发挥瑞替尼在改善预后方面的潜力。
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Unraveling Ritlecitinib: an in-depth analysis of JAK3 inhibitor for the treatment of alopecia areata.
INTRODUCTION Alopecia Areata (AA), characterized by non-scarring hair loss due to the dysregulation of the JAK/STAT pathway, has long lacked effective treatment. In 2023, Ritlecitinib, a novel Janus kinase (JAK) 3 and tyrosine kinase family inhibitor, received its first approval from the US FDA to treat AA, followed by approvals in Japan, Europe, China, and the UK. This development aims to address the challenges faced by millions of individuals affected by this condition globally. AREAS COVERED This review offers an overview of Ritlecitinib's pharmacological properties, biological targets, and development strategies. It examines its mechanism of action, pharmacokinetics, pharmacodynamics, and clinical trial insights. Additionally, it covers the drug's chemical synthesis, contraindications, drug interactions, and potential adverse effects, with special attention to its use in adolescents, pregnant women, and the elderly. EXPERT OPINION Ritlecitinib represents a significant advancement in treating AA, offering a targeted approach with promising efficacy and a favorable safety profile. While long-term safety data and real-world effectiveness studies are needed, its oral administration and efficacy in both adults and adolescents position it as a potentially transformative therapy. Ongoing research should focus on optimizing treatment strategies, identifying predictive biomarkers, and assessing cost-effectiveness to fully realize Ritlecitinib's potential in improving outcomes.
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来源期刊
Expert Opinion on Drug Metabolism & Toxicology
Expert Opinion on Drug Metabolism & Toxicology 医学-生化与分子生物学
CiteScore
7.90
自引率
2.30%
发文量
62
审稿时长
4-8 weeks
期刊介绍: Expert Opinion on Drug Metabolism & Toxicology (ISSN 1742-5255 [print], 1744-7607 [electronic]) is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles on all aspects of ADME-Tox. Each article is structured to incorporate the author’s own expert opinion on the scope for future development. The Editors welcome: Reviews covering metabolic, pharmacokinetic and toxicological issues relating to specific drugs, drug-drug interactions, drug classes or their use in specific populations; issues relating to enzymes involved in the metabolism, disposition and excretion of drugs; techniques involved in the study of drug metabolism and toxicology; novel technologies for obtaining ADME-Tox data. Drug Evaluations reviewing the clinical, toxicological and pharmacokinetic data on a particular drug. The audience consists of scientists and managers in the pharmaceutical industry, pharmacologists, clinical toxicologists and related professionals.
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