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- W2022302254 abstract "To monitor the performance of the approved generic copies of a brand-name drug, we propose some methods in assessing bioequivalence among generic copies and the brand-name drug, and among generic copies themselves, using data from several bioequivalence studies adopting the standard 2 x 2 crossover design without carryover effects. We propose a meta-analysis method that increases statistical power when the between-subject variability is not large. A nonmeta-analysis is also considered. A numerical example of applying both methods is presented for illustration." @default.
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- W2022302254 title "BIOEQUIVALENCE REVIEW FOR DRUG INTERCHANGEABILITY" @default.
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- W2022302254 doi "https://doi.org/10.1081/bip-100101189" @default.
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