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Reference Datasets for Bioequivalence Trials in a Two-Group Parallel Design

机译:两组平行设计中生物等效性试验的参考数据集

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摘要

In order to help companies qualify and validate the software used to evaluate bioequivalence trials with two parallel treatment groups, this work aims to define datasets with known results. This paper puts a total 11 datasets into the public domain along with proposed consensus obtained via evaluations from six different software packages (R, SAS, WinNonlin, OpenOffice Calc, Kinetica, EquivTest). Insofar as possible, datasets were evaluated with and without the assumption of equal variances for the construction of a 90% confidence interval. Not all software packages provide functionality for the assumption of unequal variances (EquivTest, Kinetica), and not all packages can handle datasets with more than 1000 subjects per group (WinNonlin). Where results could be obtained across all packages, one showed questionable results when datasets contained unequal group sizes (Kinetica). A proposal is made for the results that should be used as validation targets.Electronic supplementary materialThe online version of this article (doi:10.1208/s12248-014-9704-6) contains supplementary material, which is available to authorized users.
机译:为了帮助公司鉴定和验证用于通过两个平行治疗组评估生物等效性试验的软件,这项工作旨在定义具有已知结果的数据集。本文将总共11个数据集与通过六个不同软件包(R,SAS,WinNonlin,OpenOffice Calc,Kinetica,EquivTest)进行评估获得的建议共识一起放入了公共领域。在可能的情况下,在建立和不假设方差相等的情况下评估数据集,以建立90%的置信区间。并非所有软件包都提供用于假设不等方差的功能(EquivTest,Kinetica),并且并非所有软件包都可以处理每组包含1000个以上主题的数据集(WinNonlin)。在所有包都可以获得结果的地方,当数据集包含不相等的组大小时,一个结果显示出可疑的结果(Kinetica)。针对应该作为验证目标的结果提出了建议。电子补充材料本文的在线版本(doi:10.1208 / s12248-014-9704-6)包含补充材料,授权用户可以使用。

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