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VE-1902-A 是一种直接凝血酶抑制剂,具有可还原的共价作用机制,在血栓形成的啮齿动物模型中显示出疗效且出血减少。

VE-1902-A direct thrombin inhibitor with reversible covalent mechanism of action shows efficacy with reduced bleeding in rodent models of thrombosis.

机构信息

Verseon Corporation, Fremont, CA, United States of America.

Verseon Corporation, Fremont, CA, United States of America.

出版信息

Thromb Res. 2020 Jun;190:112-121. doi: 10.1016/j.thromres.2020.04.020. Epub 2020 Apr 19.

Abstract

INTRODUCTION

High incidence of bleeding events remains a key risk for patients taking anticoagulants, especially those in need of long-term combination therapy with antiplatelet agents. As a consequence, patients may not receive clinically indicated combination antithrombotic therapy. Here, we report on VE-1902, a member of a novel class of precision oral anticoagulants (PROACs) that combines effective anticoagulation with reduced bleeding in preclinical testing.

METHODS AND RESULTS

Acting through covalent, reversible active-site modification of thrombin similar to a previously described molecule [1], VE-1902 shows potency and selectivity for thrombin inhibition in human plasma comparable to clinically relevant direct thrombin inhibitors (DTI) such as argatroban and dabigatran (thrombin generation assay ETP EC = 1.3 μM compared to 0.36 μM and 0.31 μM for argatroban and dabigatran; >100-fold selectivity against related serine proteases). Unlike the current anticoagulants, VE-1902 does not significantly inhibit thrombin-mediated platelet activation in in vivo models of thrombosis. In the thrombin generation assay, the compound inhibits thrombin formation without significantly delaying the initiation phase of the clotting cascade. These features are possibly responsible for the observed reduced bleeding in tail bleeding and saphenous vein bleeding models. Consistent with this novel pharmacological profile, VE-1902 shows efficacious anticoagulation in several fibrin-driven animal models of thrombosis (arteriovenous shunt, venous stasis thrombosis, and thrombin-induced thromboembolism models), whereas it does not significantly prevent arterial occlusion in the platelet dependent FeCl model.

CONCLUSIONS

By leaving platelet activation following vascular injury mostly unaffected, VE-1902, and the PROACs more generally, represent a new generation of precision anticoagulants with reduced bleeding risk.

摘要

简介

出血事件发生率高仍然是服用抗凝药物患者的主要风险,尤其是那些需要长期联合抗血小板药物治疗的患者。因此,患者可能无法接受临床指征明确的联合抗血栓治疗。在此,我们报告了 VE-1902,它是一类新型精准口服抗凝药物(PROACs)中的一员,在临床前研究中,它兼具有效抗凝和降低出血风险的作用。

方法和结果

通过与先前描述的分子[1]类似的、针对凝血酶活性位点的共价、可逆性修饰,VE-1902 对人血浆中凝血酶的抑制作用具有效力和选择性,与临床相关的直接凝血酶抑制剂(DTI)如阿加曲班和达比加群相当(血栓生成试验 ETP EC = 1.3 μM,而阿加曲班和达比加群分别为 0.36 μM 和 0.31 μM;对相关丝氨酸蛋白酶的选择性 >100 倍)。与现有的抗凝药物不同,VE-1902 在血栓形成的体内模型中不会显著抑制凝血酶介导的血小板激活。在血栓生成试验中,该化合物抑制凝血酶形成,而不会显著延迟凝血级联反应的起始阶段。这些特征可能是观察到在尾部出血和隐静脉出血模型中出血减少的原因。与这种新型药理学特征一致,VE-1902 在几种纤维蛋白驱动的血栓形成动物模型中表现出有效的抗凝作用(动静脉分流、静脉淤滞性血栓形成和凝血酶诱导的血栓栓塞模型),而在血小板依赖性 FeCl 模型中,它不会显著防止动脉闭塞。

结论

通过使血管损伤后血小板激活基本不受影响,VE-1902 和更普遍的 PROACs 代表了新一代具有降低出血风险的精准抗凝药物。

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本文引用的文献

1
Antithrombotic Therapy for Atrial Fibrillation with Stable Coronary Disease.
N Engl J Med. 2019 Sep 19;381(12):1103-1113. doi: 10.1056/NEJMoa1904143. Epub 2019 Sep 2.
2
MAA868 locks factor XIa in a zymogen-like state.
Blood. 2019 Mar 28;133(13):1393-1394. doi: 10.1182/blood-2019-02-900480.
3
4
Reversible covalent direct thrombin inhibitors.
PLoS One. 2018 Aug 2;13(8):e0201377. doi: 10.1371/journal.pone.0201377. eCollection 2018.
6
Mechanism Action of Platelets and Crucial Blood Coagulation Pathways in Hemostasis.
Int J Hematol Oncol Stem Cell Res. 2017 Oct 1;11(4):319-327.
8
Refinement of Mouse Protocols for the Study of Platelet Thromboembolic Responses In Vivo.
Thromb Haemost. 2017 Dec;117(12):2283-2290. doi: 10.1160/TH17-04-0250. Epub 2017 Dec 6.
9
Dual Antithrombotic Therapy with Dabigatran after PCI in Atrial Fibrillation.
N Engl J Med. 2017 Oct 19;377(16):1513-1524. doi: 10.1056/NEJMoa1708454. Epub 2017 Aug 27.
10
Rivaroxaban with or without Aspirin in Stable Cardiovascular Disease.
N Engl J Med. 2017 Oct 5;377(14):1319-1330. doi: 10.1056/NEJMoa1709118. Epub 2017 Aug 27.

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