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Bayesian Estimation in Bioequivalence Study

  • Received : 20111000
  • Accepted : 20111200
  • Published : 2011.12.31

Abstract

The classical two-period, two-sequence crossover design is no longer sufficient to assess various demands in a bioequivalence study. For instance, to estimate the within-subject and between-subject variances of test and reference formulations separately, it is necessary to use a replicate design in which each subject receives at least the reference formulation in two periods. Several designs were studied to satisfy the demands. It is provided a unified Bayesian approach applicable to those study designs. The benefit of the method in the bioequivalence study is discussed.

Keywords

Acknowledgement

Supported by : Hanshin University

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