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A Multivariate Equivalence Test Based on Mahalanobis Distance with a Data-Driven Margin

Methodology 2024-06-07 v1

Abstract

Multivariate equivalence testing is needed in a variety of scenarios for drug development. For example, drug products obtained from natural sources may contain many components for which the individual effects and/or their interactions on clinical efficacy and safety cannot be completely characterized. Such lack of sufficient characterization poses a challenge for both generic drug developers to demonstrate and regulatory authorities to determine the sameness of a proposed generic product to its reference product. Another case is to ensure batch-to-batch consistency of naturally derived products containing a vast number of components, such as botanical products. The equivalence or sameness between products containing many components that cannot be individually evaluated needs to be studied in a holistic manner. Multivariate equivalence test based on Mahalanobis distance may be suitable to evaluate many variables holistically. Existing studies based on such method assumed either a predetermined constant margin, for which a consensus is difficult to achieve, or a margin derived from the data, where, however, the randomness is ignored during the testing. In this study, we propose a multivariate equivalence test based on Mahalanobis distance with a data-drive margin with the randomness in the margin considered. Several possible implementations are compared with existing approaches via extensive simulation studies.

Cite

@article{arxiv.2406.03596,
  title  = {A Multivariate Equivalence Test Based on Mahalanobis Distance with a Data-Driven Margin},
  author = {Chao Wang and Yu-Ting Weng and Shaobo Liu and Tengfei Li and Meiyu Shen and Yi Tsong},
  journal= {arXiv preprint arXiv:2406.03596},
  year   = {2024}
}
R2 v1 2026-06-28T16:55:06.322Z