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达比加群(YM150)与依诺肝素预防全髋关节置换术后静脉血栓栓塞症的随机、Ⅱb 期剂量确证研究(ONYX-3)

Darexaban (YM150) versus enoxaparin for the prevention of venous thromboembolism after total hip arthroplasty: a randomised phase IIb dose confirmation study (ONYX-3).

机构信息

Bengt I. Eriksson, MD, PhD, Sahlgrenska University Hospital, Gothenburg, Sweden, Tel: +46 31 343 4408, Fax: +46 3 187 8531, E-mail:

出版信息

Thromb Haemost. 2014 Feb;111(2):213-25. doi: 10.1160/TH13-04-0296. Epub 2013 Oct 17.

DOI:10.1160/TH13-04-0296
PMID:24136153
Abstract

This double-blind, double-dummy, randomised, phase IIb study (NCT00902928) evaluated different dosing regimens of darexaban compared with enoxaparin (randomised 1:1:1:1:1 to 15 mg twice daily [bid], 30 mg once daily [qd], 30 mg bid or 60 mg qd or enoxaparin 40 mg qd) in patients undergoing elective total hip arthroplasty. Patients, investigators, pharmacists and sponsor were all blinded to treatment allocation. Darexaban administration started 6-10 hours (h) post-surgery. Enoxaparin 40 mg qd administration started 12 ± 2 h before surgery. Treatment continued for 35 days. Bilateral venography was performed on Day 10 ± 2. The primary efficacy outcome was total VTEs (composite of proximal/distal deep-vein thrombosis, pulmonary embolism) or death, at Day 12. Total VTE rates were similar across all groups. There was no apparent difference in efficacy between once- and twice-daily darexaban (odds ratio [OR] 1.00; 95% confidence interval [CI] 0.71-1.42; p=0.988), or total daily dose (30 mg/day vs 60 mg/day; OR 0.81; 95% CI 0.57-1.15; p=0.244). There was no significant difference in major and/or clinically relevant non-major bleeding between darexaban qd or bid, or between total daily doses of 30 mg or 60 mg, and also for any dosing regimen of darexaban vs enoxaparin. Darexaban was well tolerated, without signs of liver toxicity. In conclusion, darexaban, administered qd or bid, and at total daily doses of 30 mg or 60 mg, appears to be effective for VTE prevention and was well tolerated. Data suggest no significant differences between a once- or twice-daily dosing regimen.

摘要

这项双盲、双模拟、随机、2b 期研究(NCT00902928)评估了达比加群与依诺肝素的不同给药方案(按 1:1:1:1:1 比例随机分为 15mg 每日两次[bid]、30mg 每日一次[qd]、30mg bid 或 60mg qd 或依诺肝素 40mg qd),用于接受择期全髋关节置换术的患者。患者、研究者、药剂师和赞助商均对治疗分配设盲。达比加群给药于术后 6-10 小时(h)开始。依诺肝素 40mg qd 于术前 12±2h 开始给药。治疗持续 35 天。第 10±2 天进行双侧静脉造影。主要疗效终点为第 12 天的总静脉血栓栓塞事件(近端/远端深静脉血栓形成、肺栓塞)或死亡。所有组的总静脉血栓栓塞率相似。每日一次和两次给药的达比加群(比值比[OR]1.00;95%置信区间[CI]0.71-1.42;p=0.988)或总日剂量(30mg/天与 60mg/天;OR 0.81;95%CI 0.57-1.15;p=0.244)之间在疗效上无明显差异。达比加群 qd 或 bid、30mg 或 60mg 总日剂量之间,以及与依诺肝素任何给药方案之间,主要和/或有临床意义的非主要出血无显著差异。达比加群耐受性良好,无肝毒性迹象。总之,qd 或 bid 给药,总日剂量 30mg 或 60mg,达比加群似乎对静脉血栓栓塞预防有效且耐受性良好。数据表明,每日一次或两次给药方案之间无显著差异。

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