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稳定成年肾移植受者中环孢素制剂的互换性:在一项国际多中心随机开放标签试验中对Equoral胶囊和Neoral胶囊的比较。

Interchangeability of ciclosporin formulations in stable adult renal transplant recipients: comparison of Equoral and Neoral capsules in an international, multicenter, randomized, open-label trial.

作者信息

Vítko Stefan, Ferkl Marek

机构信息

Institute for Clinical and Experimental Medicine, Prague, Czech Republic.

出版信息

Kidney Int Suppl. 2010 Mar(115):S12-6. doi: 10.1038/ki.2009.506.

Abstract

The cost of immunosuppression following transplantation can be reduced by using generic ciclosporin (for example, Equoral) rather than innovator ciclosporin drugs such as Neoral. Thus, this study aims to evaluate the interchangeability, safety, and tolerability of Equoral, a generic ciclosporin, with Neoral in stable adult renal transplant recipients. This was a multicenter, randomized, open-label, parallel-group clinical trial in stable renal transplant patients, comparing 6 months of treatment with Equoral with the same treatment period on Neoral. The primary end point was the between-treatment comparison of the total daily ciclosporin dose at the end of the study. A total of 99 patients were enrolled and constituted the full analysis/safety population, and 78 patients forming the per-protocol population were assessed for efficacy. Equoral was found to be equivalent to Neoral with regard to the primary end point of daily dose at the end of the study. This was supported by comparable serum ciclosporin levels at the end of the study. There were no renal transplant rejection incidents, but there was one death (in the Neoral group). Drug tolerability and incidence of adverse events were comparable between the treatment groups. In conclusion, Equoral and Neoral are interchangeable in stable renal transplant patients, and both drugs are associated with a similar safety and tolerability profile.

摘要

使用环孢素通用制剂(如Equoral)而非Neoral等创新型环孢素药物,可降低移植后免疫抑制的成本。因此,本研究旨在评估通用型环孢素Equoral与Neoral在稳定的成年肾移植受者中的互换性、安全性和耐受性。这是一项针对稳定肾移植患者的多中心、随机、开放标签、平行组临床试验,比较Equoral治疗6个月与Neoral相同治疗期的效果。主要终点是研究结束时每日环孢素总剂量的治疗组间比较。共纳入99例患者,构成完整分析/安全人群,78例符合方案人群的患者接受了疗效评估。研究发现,在研究结束时每日剂量的主要终点方面,Equoral与Neoral相当。研究结束时可比的血清环孢素水平也支持了这一点。未发生肾移植排斥事件,但有1例死亡(在Neoral组)。治疗组之间的药物耐受性和不良事件发生率相当。总之,在稳定的肾移植患者中,Equoral和Neoral可互换,且两种药物的安全性和耐受性相似。

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