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安多凝血酶原片段2用于接受直接和间接Xa因子抑制剂治疗的患者抗凝活性的逆转。

Andexanet alfa for the reversal of anticoagulant activity in patients treated with direct and indirect factor Xa inhibitors.

作者信息

Nafee Tarek, Aslam Aysha, Chi Gerald, Pahlavani Seyedmahdi, Nimri Dima, Kuchkuntla Aravind Reddy, Talib Usama, Michalak Nathan, Daaboul Yazan, Korjian Serge, Gallo Anthony, Gibson C Michael

机构信息

a PERFUSE Study Group, Cardiovascular Division, Department of Medicine , Beth Israel Deaconess Medical Center, Harvard Medical School , Boston , MA , USA.

出版信息

Expert Rev Cardiovasc Ther. 2017 Apr;15(4):237-245. doi: 10.1080/14779072.2017.1305889. Epub 2017 Mar 22.

Abstract

Andexanet alfa is a recombinant factor Xa decoy molecule that inhibits direct and indirect factor Xa inhibitors to allow the normal coagulation process to resume. Its development arises in a space where novel oral anticoagulants are receiving expanded indications yet their use is limited by the lack of an effective reversal agent. Areas covered: This article reviews the biochemical properties, mechanism of action and the preclinical and clinical trials on andexanet alfa. It additionally aims to provide expert commentary and future perspectives on the efficacy, safety and challenges facing andexanet alfa as a universal antidote for direct and indirect factor Xa inhibitors. Expert commentary: Andexanet alfa shows promise to become a highly effective, novel antidote for factor Xa anticoagulation. Its biochemical profile and mechanism of action are immediately more attractive than other drugs on the market and under development due to its inert nature within the normal coagulation cascade, with minimal intrinsic procoagulant or anticoagulant properties. The anticoagulant antidote space will continue to develop as more specific and universal options become available for reversal of the effect of DOACs. Preliminary results of a pivotal phase 3b/4 trial demonstrate a favorable efficacy and safety profile in patients with acute hemorrhage.

摘要

andexanet alfa是一种重组Xa因子诱饵分子,可抑制直接和间接Xa因子抑制剂,使正常凝血过程得以恢复。它的研发源于一个新的领域,即新型口服抗凝药的适应证不断扩大,但其使用却因缺乏有效的逆转剂而受到限制。涵盖领域:本文综述了andexanet alfa的生化特性、作用机制以及临床前和临床试验情况。此外,本文旨在就andexanet alfa作为直接和间接Xa因子抑制剂的通用解毒剂在疗效、安全性和面临的挑战方面提供专家评论和未来展望。专家评论:andexanet alfa有望成为一种高效的新型Xa因子抗凝解毒剂。由于其在正常凝血级联反应中具有惰性,内在促凝或抗凝特性极小,其生化特征和作用机制比市场上和正在研发的其他药物更具吸引力。随着越来越多特异性和通用性更强的药物可用于逆转直接口服抗凝药(DOACs)的作用,抗凝解毒剂领域将持续发展。一项关键的3b/4期试验的初步结果显示,该药在急性出血患者中具有良好的疗效和安全性。

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