Design and Analysis of Method Equivalence Studies

被引:42
作者
Borman, Phil J. [1 ]
Chatfield, Marion J. [1 ]
Damjanov, Ivana [1 ]
Jackson, Patrick [1 ]
机构
[1] GlaxoSmithKline Med Res Ctr, Stevenage SG1 2NY, Herts, England
关键词
D O I
10.1021/ac901945f
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Method equivalence assessments should be considered when analytical methods are either modified or substituted. The TOST (two one sided tests) approach provides a sounder data driven method for testing equivalence than a simple comparative intermediate precision study which is typically performed as part of method validation. Prior to designing an equivalency study, an acceptance criterion (an acceptable bias between original and modified/changed method) must be chosen. The choice of acceptance criteria requires the identification of the smallest mean difference or bias between methods that is practically important. Equivalence testing in this manner is used to prove that the new method can generate data which continues to support previously established specifications. Once the acceptance criterion is decided, other aspects of the study can be designed following a set of design principles. When the design and acceptance criteria have been established, the collection of the data can commence. Demonstration of equivalence should not start until the validity of the observations has been confirmed such as assessment for outliers, normality, and comparison of variances. Once the suitability of the data is confirmed, the mean difference between the two data sets can be calculated along with a +/- 90% confidence interval using the TOST approach. It can then be established whether equivalence of the two methods has been demonstrated.
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收藏
页码:9849 / 9857
页数:9
相关论文
共 14 条
[1]   MEASUREMENT IN MEDICINE - THE ANALYSIS OF METHOD COMPARISON STUDIES [J].
ALTMAN, DG ;
BLAND, JM .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES D-THE STATISTICIAN, 1983, 32 (03) :307-317
[2]  
Borman P., 2007, Pharm. Technol, V31, P142
[3]  
CHATFIELD MJ, ANAL CHEM, DOI DOI 10.1021/AC901944F
[4]   Analytical method transfer: New descriptive approach for acceptance criteria definition [J].
de Fontenay, Gerald .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2008, 46 (01) :104-112
[5]  
Ermer J, 2005, METHOD VALIDATION IN PHARMACEUTICAL ANALYSIS: A GUIDE TO BEST PRACTICE, P1
[6]  
Hahn G. J., 1991, STAT INTERVALS GUIDE
[7]  
*ICH, 2008, ICH TOP Q8 R1 PHARM
[8]   Some practical guidelines for effective sample size determination [J].
Lenth, RV .
AMERICAN STATISTICIAN, 2001, 55 (03) :187-193
[9]   Beyond the t-test:: Statistical equivalence testing. [J].
Limentani, GB ;
Ringo, MC ;
Ye, F ;
Bergquist, ML ;
McSorley, EP .
ANALYTICAL CHEMISTRY, 2005, 77 (11) :221A-226A
[10]   Kurtosis provides a good omnibus test for outliers in small samples [J].
Livesey, John H. .
CLINICAL BIOCHEMISTRY, 2007, 40 (13-14) :1032-1036