因子XI/XIa抑制剂:抗凝困境的潜在解决方案。

IF 2.7 3区 医学 Q3 PHARMACOLOGY & PHARMACY
Expert Opinion on Pharmacotherapy Pub Date : 2025-04-01 Epub Date: 2025-03-05 DOI:10.1080/14656566.2025.2475192
Caitlin M Gibson, Umesh R Desai, Megan E Wesling
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引用次数: 0

摘要

抗血栓治疗是预防中风的基础,但标准治疗未得到充分利用,并且由于出血率、药物相互作用和肾脏消除而限制了其使用。因子XI/XIa (FXI/XIa)抑制剂是一种新型抗凝类药物,据称针对血栓形成而不是止血,从而提高了在保持疗效的同时减少出血后果的希望。涵盖领域:本综述涵盖了FXI/XIa抑制剂的机制原理,描述了各种分子亚类,解决了当前抗凝使用的障碍,并回顾了迄今为止这类新型抗凝剂的临床试验数据。专家意见:与doac相比,FXI/XIa抑制剂在卒中预防方面有几个优势,如减少出血、药物相互作用少、肾脏消除少。然而,与doac相比,临床试验必须证明其疗效不差,安全性更高。其他使用障碍包括成本、解毒剂不足和抗凝剂的全面利用不足。小分子或单克隆抗体进入临床的可能性非常高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Factor XI/XIa inhibitors: a potential solution to anticoagulation dilemmas.

Introduction: Antithrombotic therapy is the cornerstone of stroke prevention, but standard of care therapies are underutilized and use is limited by bleeding rates, drug interactions, and renal elimination. Factor XI/XIa (FXI/XIa) inhibitors are a novel anticoagulation class that purportedly target thrombosis more than hemostasis, thereby raising the hope of reducing bleeding consequences while maintaining efficacy.

Areas covered: This review covers the mechanistic rationale for FXI/XIa inhibitors, describes the various molecule sub-classes, addresses barriers to current anticoagulation use, and reviews clinical trial data to date for this novel class of anticoagulants.

Expert opinion: FXI/XIa inhibitors offer several advantages over DOACs in stroke prevention such as reduced bleeding, fewer drug interactions, and less renal elimination. However, clinical trials must demonstrate non-inferior efficacy and improved safety compared to DOACs. Additional barriers to use will include cost, inadequacy of antidotes, and overall anticoagulant underutilization. The potential for a small molecule or monoclonal antibody to reach the clinic is very high.

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来源期刊
CiteScore
5.60
自引率
3.10%
发文量
163
审稿时长
4-8 weeks
期刊介绍: Expert Opinion on Pharmacotherapy is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles and original papers on newly approved/near to launch compounds mainly of chemical/synthetic origin, providing expert opinion on the likely impact of these new agents on existing pharmacotherapy of specific diseases.
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