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Evaluation of a Scaling Approach for the Bioequivalence of Highly Variable Drugs

Various approaches for evaluating the bioequivalence (BE) of highly variable drugs (CV ≥ 30%) have been debated for many years. More recently, the FDA conducted research to evaluate one such approach: scaled average BE. A main objective of this study was to determine the impact of scaled average BE...

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Main Authors: Haidar, Sam H., Makhlouf, Fairouz, Schuirmann, Donald J., Hyslop, Terry, Davit, Barbara, Conner, Dale, Yu, Lawrence X.
格式: Artigo
語言:Inglês
出版: Springer US 2008
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC2761698/
https://ncbi.nlm.nih.gov/pubmed/18726698
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1208/s12248-008-9053-4
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