Confidence region approach for assessing bioequivalence and biosimilarity accounting for heterogeneity of variability

Published

Journal Article

© 2015 Jianghao Li and Shein-Chung Chow. For approval of generic drugs, the FDA requires that evidence of bioequivalence in average bioequivalence in terms of drug absorption be provided through the conduct of a bioequivalence study. A test product is said to be average bioequivalent to a reference (innovative) product if the 90% confidence interval of the ratio of means (after log-transformation) is totally within (80%, 125%). This approach is considered a one-parameter approach, which does not account for possible heterogeneity of variability between drug products. In this paper, we study a two-parameter approach (i.e., confidence region approach) for assessing bioequivalence, which can also be applied to assessing biosimilarity of biosimilar products. The proposed confidence region approach is compared with the traditional one-parameter approach both theoretically and numerically (i.e., simulation study) for finite sample performance.

Full Text

Duke Authors

Cited Authors

  • Li, J; Chow, SC

Published Date

  • January 1, 2015

Published In

Volume / Issue

  • 2015 /

Electronic International Standard Serial Number (EISSN)

  • 1687-9538

International Standard Serial Number (ISSN)

  • 1687-952X

Digital Object Identifier (DOI)

  • 10.1155/2015/298647

Citation Source

  • Scopus