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探索凝血因子XIa抑制剂阿孙德西安的治疗效用。

Exploring the therapeutic utility of the factor XIa inhibitor asundexian.

作者信息

Edwards Jocelyn, Corey Jack, Coons James C

机构信息

ChristianaCare, Newark, DE, USA.

Ochsner LSU Health Shreveport, Shreveport, LA, USA.

出版信息

Am J Health Syst Pharm. 2024 Dec 5;81(24):1222-1229. doi: 10.1093/ajhp/zxae182.

Abstract

PURPOSE

Factor XIa inhibitors are a promising novel class of anticoagulants that attenuate pathological thrombosis with minimal interference with hemostasis. These effects contrast with those of conventional anticoagulants, which may exhibit adverse events of untoward bleeding precluding treatment in some patients. A variety of investigational pharmacological modalities have been developed and studied to target factor XIa.

SUMMARY

Asundexian is a small molecule inhibitor of factor XIa that has been evaluated in several clinical studies. It has been studied as an oral, once-daily medication and found to inhibit approximately 90% of factor XIa activity at doses of 20 to 50 mg. Phase 2 trials have demonstrated the potential for improved safety compared to standard of care in certain treatment settings, such as in atrial fibrillation. For other indications, such as noncardioembolic stroke and acute myocardial infarction, asundexian has been used in addition to background antiplatelet therapy. In these instances, asundexian did not show a difference in the incidence of bleeding events compared to placebo.

CONCLUSION

Phase 3 trials have recently been launched; however, the OCEANIC-AF trial was prematurely discontinued due to inefficacy of asundexian vs apixaban for stroke prevention in atrial fibrillation. Another phase 3 trial, OCEANIC-AFINA, is planned to compare asundexian to placebo in patients with atrial fibrillation at high risk for stroke who are deemed ineligible for anticoagulation.

摘要

目的

凝血因子Ⅺa抑制剂是一类很有前景的新型抗凝剂,能在对止血干扰最小的情况下减轻病理性血栓形成。这些作用与传统抗凝剂不同,传统抗凝剂可能会出现不良出血事件,导致一些患者无法接受治疗。目前已开发并研究了多种针对凝血因子Ⅺa的研究性药理方法。

总结

阿孙地昔是一种凝血因子Ⅺa小分子抑制剂,已在多项临床研究中进行了评估。它被作为一种每日一次的口服药物进行研究,发现在20至50毫克剂量下可抑制约90%的凝血因子Ⅺa活性。2期试验已证明,在某些治疗环境中,如心房颤动,与标准治疗相比,其安全性有改善的潜力。对于其他适应症,如非心源性卒中及急性心肌梗死,阿孙地昔在背景抗血小板治疗基础上使用。在这些情况下,与安慰剂相比,阿孙地昔在出血事件发生率上没有差异。

结论

最近已启动3期试验;然而,由于在心房颤动中风预防方面阿孙地昔对比阿哌沙班无效,OCEANIC-AF试验提前终止。另一项3期试验OCEANIC-AFINA计划在被认为不适合抗凝治疗的高卒中风险心房颤动患者中,将阿孙地昔与安慰剂进行比较。

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