Ximelagatran: a new oral anticoagulant.

Lenka Hrebickova, James J Nawarskas, Joe R Anderson
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引用次数: 14

Abstract

Although there have been many significant advances over the last 50 years with regards to anticoagulant therapy, warfarin remains the definitive standard for the long-term prevention of thromboembolic events in many patients at risk for these complications. Although effective, warfarin has a narrow therapeutic window, necessitating frequent laboratory monitoring for anticoagulant effect. Ximelagatran is an investigational anticoagulant that directly inhibits thrombin, unlike heparin or warfarin, which are indirect inhibitors. Although indirect thrombin inhibitors are mainly only effective at inhibiting circulating thrombin, direct thrombin inhibitors are able to inhibit both free and clot-bound thrombin, thereby producing more effective anticoagulation. Ximelagatran is the first orally available direct thrombin inhibitor to reach phase 3 clinical trials. Ximelagatran is a prodrug for the active metabolite melagatran, and has been demonstrated to have a relatively wide therapeutic window in terms of bleeding and antithrombotic effect compared with warfarin. Clinical studies have demonstrated ximelagatran to be comparable in efficacy to warfarin and low-molecular-weight heparins (LMWH) for prophylaxis of venous thromboembolism, comparable to warfarin for stroke prevention in the setting of atrial fibrillation, and, when combined with aspirin, possible more effective than aspirin alone at preventing major adverse cardiovascular events in patients with a recent myocardial infarction. Adverse effects with ximelagatran primarily involve bleeding complications, which are more frequent than with placebo, but appear comparable to those occurring with standard anticoagulant treatment (ie, warfarin and LMWH). Ximelagatran has also been demonstrated to cause transient increases in liver enzymes, the significance of which will need to be addressed in ongoing phase 3 studies. Should ongoing trials prove ximelagatran to have at least similar therapeutic efficacy and safety as warfarin, ximelagatran may become a first-line anticoagulant due to its ease of administration and lack of a need for drug monitoring. The results of these trials are eagerly awaited in helping to defining the place in therapy for this promising new agent.

一种新型口服抗凝剂。
尽管在过去的50年里,抗凝治疗取得了许多重大进展,华法林仍然是许多有并发症风险的患者长期预防血栓栓塞事件的最终标准。华法林虽然有效,但治疗窗口较窄,需要经常在实验室监测抗凝效果。Ximelagatran是一种研究性抗凝血剂,直接抑制凝血酶,不像肝素或华法林是间接抑制剂。虽然间接凝血酶抑制剂主要只对循环凝血酶有效,但直接凝血酶抑制剂能够同时抑制游离凝血酶和凝块结合凝血酶,从而产生更有效的抗凝作用。Ximelagatran是第一个达到3期临床试验的口服直接凝血酶抑制剂。Ximelagatran是活性代谢物melagatran的前药,与华法林相比,已被证明在出血和抗血栓作用方面具有相对较宽的治疗窗口。临床研究表明,在预防静脉血栓栓塞方面,ximelagatran的疗效与华法林和低分子肝素(LMWH)相当,在房颤的情况下,与华法林预防卒中的疗效相当,并且,当与阿司匹林联合使用时,在预防近期心肌梗死患者的主要不良心血管事件方面可能比阿司匹林单独使用更有效。ximelagatran的不良反应主要包括出血并发症,这比安慰剂更常见,但与标准抗凝治疗(即华法林和低分子肝素)发生的情况相当。Ximelagatran也被证明可以引起肝酶的短暂性增加,其重要性需要在正在进行的3期研究中得到解决。如果正在进行的试验证明ximelagatran至少具有与华法林相似的治疗效果和安全性,则由于其易于给药和不需要药物监测,ximelagatran可能成为一线抗凝血剂。这些试验的结果被急切地等待着,以帮助确定这种有前途的新药在治疗中的位置。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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