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Efficacy and safety of a conversion from the original tacrolimus and mycophenolate mofetil to the generics Tacpan? and Mowel? after liver transplantation

机译:肝移植后从原始他克莫司和霉酚酸酯转化为仿制药Tacpan ?和Mowel ?的功效和安全性

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Background: Expensive pharmaceuticals are a major reason for cost intensive health care systems. Long-term immunosuppressive therapy plays a relevant role after organ transplantation. Patents of original drugs have expired and cheaper products are available. Little data are available regarding efficacy and safety of generic immunosuppressive agents. Methods: In this prospective study, 25 patients, who were clinically stable for a minimum of 2 years after liver transplantation, were converted from the original formulations of tacrolimus (TAC) and mycophenolate mofetil to the generics Tacpan? (TAP) and Mowel? (MOW). Patients were followed-up for 6 months. Results were compared retrospectively to 25 age- and sex-matched controls treated with the original brands. Results: In the matched-pair analysis of TAC trough level/dose ratio, no significant difference was found between TAP/MOW and TAC/mycophenolate mofetil groups. No acute rejection occurred in either group. In total, 17 patients reported mild side effects in the TAP/MOW group. The most common side effects were gastrointestinal symptoms. Intra-individual analysis of costs revealed a considerable cost reduction in the TAP/MOW group (in median 25.03%; P <0.001). Conclusion: In summary, the use of the generics TAP/MOW is effective and seems to be safe and cost-efficient in stable liver-transplantation patients.
机译:背景:昂贵的药品是成本密集型医疗保健系统的主要原因。器官移植后,长期的免疫抑制治疗起着重要的作用。原药专利已经过期,并且可以找到更便宜的产品。关于通用免疫抑制剂的功效和安全性的数据很少。方法:在这项前瞻性研究中,将25例肝移植后至少两年内临床稳定的患者从他克莫司(TAC)和霉酚酸酯的原始配方转换为仿制药Tacpan ? (TAP)和Mowel ?(MOW)。对患者进行了6个月的随访。将结果与使用原始品牌治疗的25个年龄和性别匹配的对照进行比较。结果:在TAC谷水平/剂量比的配对分析中,TAP / MOW组和TAC /霉酚酸酯组之间无显着差异。两组均未发生急性排斥反应。在TAP / MOW组中,总共有17位患者报告了轻微的副作用。最常见的副作用是胃肠道症状。成本内的个人分析表明,TAP / MOW组的成本显着降低(中位数为25.03%; P <0.001)。结论:总而言之,在稳定的肝移植患者中使用仿制药TAP / MOW是有效的,并且似乎是安全且具有成本效益的。

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