Reversal Agents in Development for the New Oral Anticoagulants

被引:32
作者
Costin, James [1 ]
Ansell, Jack [2 ]
Laulicht, Bryan [1 ]
Bakhru, Sasha [1 ]
Steiner, Solomon [1 ]
机构
[1] Perosphere Inc, Danbury, CT 06810 USA
[2] Hofstra North Shore Long Isl Jewish Sch Med, Hempstead, NY USA
关键词
anticoagulation; reversal; atrial fibrillation; stroke; gastrointestinal bleed; PER977; new oral anticoagulants; ATRIAL-FIBRILLATION; ANTIDOTE; MANAGEMENT;
D O I
10.3810/pgm.2014.11.2829
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The new oral anticoagulants have many advantages over vitamin K antagonists, but they are still associated with a troublesome incidence of major bleeding. Additionally, the absence of a reversal agent for the new oral anticoagulants is a barrier to their more widespread use. Currently, there are 3 potential reversal agents in development: idarucizumab is a humanized murine monoclonal antibody fragment directed specifically at dabigatran; andexanet alfa is a recombinant modified decoy factor Xa that binds to factor Xa inhibitors; and PER977 is a small molecule that binds to factor Xa and IIa inhibitors and to heparin-based anticoagulants through charge interaction. These agents have undergone phase I clinical testing, appear to be well tolerated in healthy volunteers, and are effective in neutralizing their respective targets. All 3 are currently undergoing or entering into a phase II or III clinical study. This article reviews the available data for idarucizumab, andexanet alfa, and PER977.
引用
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页码:19 / 24
页数:6
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