On robust estimation using individual ratios in bioavailability trials

DOI10.1080/03610929408831271MaRDI QIDQ4843746zbMATH OpenOpenAlexFDO

Authors Lianng Yuh, Stephen J. Ruberg

Publication date 17 August 1995

Published in Communications in Statistics: Theory and Methods (Search for Journal in Brave)

Full work available at URL https://doi.org/10.1080/03610929408831271

zbMATH Keywords

\(t\)-distributionheavy-tailedmaximum likelihoodmedianskewed

Mathematics Subject Classification ID

Statistics (62-XX)

Recommendations

• Interval Estimation for Ratios in Bioequivalence Trials
• Optimizing sample size in relative bioavailability trials using a Bayesian decision-theoretic framework
• A nearly unbiased test for individual bioequivalence problems using probability criteria
• Doubly robust estimation of optimal dosing strategies
• Robustness of the shrinkage estimator for the relative potency in the combination of multivariate bioassays

Cites work

• On Adaptive M-Regression
• Robust Estimation of a Location Parameter
• Robust Statistics

Cited in

(1)

• Cross-product ratio calculation under different sampling schemes in clinical trials -- case study of the CYP-GUIDES trial

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