Gueret P, Combe S, Krezel C, Fuseau E, van Giersbergen P L M, Petitou M, Neuhart E
Haemostasis Department, University Hospital Pontchaillou, 2 rue Henri Le Guilloux, 35033, Rennes Cedex, France.
GETBO EA 3878, Brest, France.
Eur J Clin Pharmacol. 2017 Jan;73(1):15-28. doi: 10.1007/s00228-016-2143-9. Epub 2016 Oct 15.
EP217609 is a representative of a new class of synthetic parenteral anticoagulants with a dual mechanism of action. It combines in a single molecule a direct thrombin inhibitor and an indirect factor Xa inhibitor. EP217609 can be neutralized by a specific antidote avidin, which binds to the biotin moiety of EP217609.
The primary objective was to assess the neutralization of EP217609 by avidin in healthy subjects. Secondary objectives were to define the optimal avidin monomer/EP217609 molar ratio to achieve an adequate neutralization of EP217609 and to assess the safety and tolerability of EP217609 and avidin.
Healthy subjects (n = 36) were randomized to a 3 by 3 replicated Latin square design between 3 EP217609 doses (4, 8, 12 mg) and 3 avidin monomer/EP217609 molar ratios (1:1; 2:1; 3:1). EP217609 was administered as a single intravenous bolus, and avidin as a 30-min intravenous infusion, starting 90 min after EP217609 administration.
Overall, EP217609 and avidin were well tolerated. One subject experienced a benign and transient typical pseudo-allergic reaction. The administration of EP217609 resulted in dose-dependent increases in pharmacodynamic markers. Avidin triggered a rapid and irreversible neutralization of EP217609 without rebound effect. Adequate neutralization of the anticoagulant activity was achieved with both 2:1 and 3:1 avidin monomer/EP217609 molar ratios. All safety parameters did not show any treatment-emergent clinically relevant changes or abnormalities in any dose group.
These results will allow further investigation in patients requiring a neutralizable anticoagulant as those undergoing cardiac surgery.
EudraCT number 2010-020216-10.
EP217609是一类新型合成胃肠外抗凝剂的代表,具有双重作用机制。它在单个分子中结合了直接凝血酶抑制剂和间接Xa因子抑制剂。EP217609可被特异性解毒剂抗生物素蛋白中和,抗生物素蛋白与EP217609的生物素部分结合。
主要目的是评估健康受试者中抗生物素蛋白对EP217609的中和作用。次要目的是确定实现对EP217609充分中和的最佳抗生物素蛋白单体/EP217609摩尔比,并评估EP217609和抗生物素蛋白的安全性和耐受性。
健康受试者(n = 36)被随机分配到3×3重复拉丁方设计中,涉及3种EP217609剂量(4、8、12毫克)和3种抗生物素蛋白单体/EP217609摩尔比(1:1;2:1;3:1)。EP217609作为单次静脉推注给药,抗生物素蛋白在EP217609给药90分钟后开始进行30分钟静脉输注。
总体而言,EP217609和抗生物素蛋白耐受性良好。一名受试者经历了良性且短暂的典型类过敏反应。EP217609的给药导致药效学标志物呈剂量依赖性增加。抗生物素蛋白引发了对EP217609的快速且不可逆的中和,无反弹效应。抗生物素蛋白单体/EP217609摩尔比为2:1和3:1时均可实现对抗凝活性的充分中和。所有安全参数在任何剂量组中均未显示出任何治疗中出现的临床相关变化或异常。
这些结果将有助于对需要可中和抗凝剂的患者(如接受心脏手术的患者)进行进一步研究。
欧洲临床试验数据库编号2010 - 020216 - 10。