A note on sample size determination for bioequivalence studies with high-order crossover designs.
Similar to Liu and Chow, approximate formulas for sample size determination are derived based on Schuirmann's two one-sided tests procedure for bioequivalence studies for the additive and the multiplicative models under various higher order crossover designs for comparing two formulations of a drug product. The higher order crossover designs under study include Balaam's design, the two-sequence dual design, and two four-period designs (with two and four sequences), which are commonly used for assessment of bioequivalence between formulations. The derived formulas are simple enough to be carried out with a pocket calculator. The number of subjects required for each of the four higher order designs are tabulated for selected powers and various parameter values.
Duke Scholars
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Related Subject Headings
- Therapeutic Equivalency
- Sample Size
- Pharmacology & Pharmacy
- Humans
- Cross-Over Studies
- Clinical Trials as Topic
- 3214 Pharmacology and pharmaceutical sciences
- 1115 Pharmacology and Pharmaceutical Sciences
Citation
Published In
DOI
ISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- Therapeutic Equivalency
- Sample Size
- Pharmacology & Pharmacy
- Humans
- Cross-Over Studies
- Clinical Trials as Topic
- 3214 Pharmacology and pharmaceutical sciences
- 1115 Pharmacology and Pharmaceutical Sciences