A Bayesian framework for virtual comparative trials and bioequivalence assessments

IntroductionIn virtual bioequivalence (VBE) assessments, pharmacokinetic models informed with in vitro data and verified with small clinical trials' data are used to simulate otherwise unfeasibly large trials. Simulated VBE trials are assessed in a frequentist framework as if they were real des...

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Bibliographic Details
Main Authors: Frederic Y. Bois (Author), Céline Brochot (Author)
Format: Book
Published: Frontiers Media S.A., 2024-07-01T00:00:00Z.
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