In comparative bioavailability trials, the focus in the determination of bioequivalence has been to show that the average bioavailability on a test formulation is similar to the average bioavailability on a reference formulation. It has been argued that this is not adequate to insure interchangeability of formulations. We introduce a moment-based criterion which ensures interchangeability for at least a certain proportion of the population. An algorithm is given for determining the constant in the criterion. An example is used to illustrate how the criterion may be applied.
No takes yet. Share an insight, caveat, or question.
Holder et al. (1993) studied this question.
Synapse has enriched one closely related paper. Consider it for comparative context: