Testing for bioequivalence of highly variable drugs from TR-RT crossover designs with heterogeneous residual variances
Author:
Affiliation:
1. The Statistical Intelligence Group LLC; Manhattan KS USA
2. Department of Statistics; Kansas State University; Manhattan KS USA
Publisher
Wiley
Subject
Pharmacology (medical),Pharmacology,Statistics and Probability
Reference56 articles.
1. International Guidelines for Bioequivalence of Systemically Available Orally Administered Generic Drug Products: A Survey of Similarities and Differences
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2. An iterative method to protect the type I error rate in bioequivalence studies under two‐stage adaptive 2×2 crossover designs;Biometrical Journal;2020-10
3. Investigation Planning and Bioequivalence evaluation of Angiotensin II Receptor Antagonists;Pharmaceutical Chemistry Journal;2019-11
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