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移植医学中的仿制药:含霉酚酸酯的创新产品与替代产品的随机比较

Generics in transplantation medicine: Randomized comparison of innovator and substitution products containing mycophenolate mofetil
.

作者信息

Reigner Bruno, Grange Susan, Bentley Darren, Banken Ludger, Abt Markus, Hughes Richard, Scheubel Emmanuel, Guentert Theodor W

出版信息

Int J Clin Pharmacol Ther. 2019 Oct;57(10):506-519. doi: 10.5414/CP203487.

Abstract

OBJECTIVE

Mycophenolate mofetil (MMF) is widely used as an immunosuppressant for the prophylaxis of acute organ rejection in recipients of solid organ transplants.

MATERIALS AND METHODS

We have compared, in healthy subjects, the pharmacokinetics of mycophenolic acid when MMF was administered in the form of the innovator product CellCept (F. Hoffmann-La Roche Ltd.) or one of three commercially available generics, Renodapt (Biocon Ltd.), Mycept (Panacea Biotec), or Cellmune (Cipla Ltd.). The study was powered to detect a 20% difference in mean formulation performance measures, but not to formally evaluate bioequivalence. Geometric mean ratios of maximum concentrations (C) and areas under plasma concentration-time curves were calculated.

RESULTS

Comparing generics against each other, the differences in point estimates of the geometric mean ratios of C of two of the comparisons were either borderline within (Renodapt/Cellmune) or clearly outside (Mycept/Cellmune) a region of 80 - 125% around the reference mean, indicating that bioequivalence between these generics may be difficult to show.

CONCLUSION

Physicians in the field of transplantation should be aware of the potential risk of altering the therapeutic outcome when switching from one preparation of MMF to another. ClinicalTrials.gov identifier: NCT02981290.

摘要

目的

霉酚酸酯(MMF)被广泛用作免疫抑制剂,用于预防实体器官移植受者的急性器官排斥反应。

材料与方法

我们在健康受试者中比较了以创新产品骁悉(F. Hoffmann-La Roche Ltd.)或三种市售仿制药之一(如:Renodapt(Biocon Ltd.)、Mycept(Panacea Biotec)或Cellmune(Cipla Ltd.))的形式给药时霉酚酸的药代动力学。该研究旨在检测平均制剂性能指标中20%的差异,但未对生物等效性进行正式评估。计算了最大浓度(C)和血浆浓度-时间曲线下面积的几何平均比值。

结果

将各仿制药相互比较时,其中两项比较的C几何平均比值的点估计差异,在参考均值周围80%-125%的区域内,要么处于临界状态(Renodapt/Cellmune),要么明显超出该区域(Mycept/Cellmune),这表明这些仿制药之间可能难以显示生物等效性。

结论

移植领域的医生应意识到从一种MMF制剂换用另一种制剂时改变治疗效果的潜在风险。ClinicalTrials.gov标识符:NCT02981290。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3aef/6751510/cff18809a267/intjclinpharmacol-57-506-01.jpg

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