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首页> 外文期刊>BMC Cardiovascular Disorders >Design and rationale for the WARFA trial: a randomized controlled cross-over trial testing the therapeutic equivalence of branded and generic warfarin in atrial fibrillation patients in Brazil
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Design and rationale for the WARFA trial: a randomized controlled cross-over trial testing the therapeutic equivalence of branded and generic warfarin in atrial fibrillation patients in Brazil

机译:WARFA试验的设计和依据:一项随机对照的交叉试验,用于测试品牌和普通华法林在巴西房颤患者中的治疗等效性

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Background Warfarin is a commonly used anticoagulant. Whether a given dose of the different formulations of Brazilian warfarin will result in the same effect on the international normalized ratio (INR) is uncertain. The aim of the WARFA trial is to determine whether the branded and two generic warfarins available in Brazil differ in their effect on the INR. Methods WARFA is a cross-over RCT comparing three warfarins. The formulations tested are the branded Marevan? (Uniao Quimica/Farmoquimica) and two generic warfarin (manufactured respectively by Uniao Quimica Farmaceutica Nacional and Laboratorio Teuto Brasileiro). All of them were manufactured in Brazil, are available in all settings of the Brazilian healthcare system and were purchased from retail drugstores. Eligible participants had atrial fibrillation or flutter, had been using warfarin for at least 2?months with a therapeutic range of 2.0–3.0 and had low variability in INR results during the 1st period?of the trial. Our primary outcome, for which we have an equality hypothesis, is the difference between warfarins in the mean absolute difference between two INR?results, obtained after three and 4 weeks with each drug. Our secondary outcomes, that will be tested for inequality (except for the mean INR, which will be tested for equality), include the difference in the warfarin dose, and time in therapeutic range. Clinical events and adherence were also recorded and will be reported. Discussion To our knowledge, WARFA will be the first comparison of the more readily applicable INR results between branded and generic warfarins in Brazil. WARFA is important because warfarins are commonly switched between in the course of a chronic treatment in Brazil. Final results of WARFA are expected in May 2017. Trial registration ClinicalTrials.gov NCT02017197 . Registered 11 December 2013.
机译:背景华法林是一种常用的抗凝剂。不确定给定剂量的巴西华法令不同制剂是否会对国际标准化比率(INR)产生相同的影响。 WARFA试验的目的是确定巴西提供的品牌和两种仿制华法林对INR的作用是否不同。方法WARFA是比较三种华法林的交叉RCT。测试的配方是Marevan品牌的吗? (Uniao Quimica / Farmoquimica)和两种仿制药华法林(分别由Uniao Quimica Farmaceutica Nacional和Laboratorio Teuto Brasileiro制造)。它们全部在巴西制造,可在巴西医疗保健系统的所有环境中使用,并从零售药店购买。符合条件的受试者患有房颤或扑动,使用华法林至少2个月,治疗范围为2.0-3.0,并且在试验的第一阶段中INR结果的变异性较低。我们有一个相等假设的主要结果是,华法林之间的差异是两种药物在三和四周后获得的两个INR结果的平均绝对差。我们的次要结果(将测试不平等程度)(平均INR(将被测试是否相等)除外)包括华法林剂量的差异以及治疗时间的长短。还记录了临床事件和依从性,并将进行报告。讨论据我们所知,WARFA将是巴西品牌华法林和通用华法林之间更容易应用的INR结果的第一个比较。 WARFA很重要,因为在巴西的长期治疗过程中,华法林通常在两者之间转换。预计WARFA的最终结果将于2017年5月发布。试用注册ClinicalTrials.gov NCT02017197。 2013年12月11日注册。

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