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Two-stage designs in bioequivalence trials.
Schütz H. Schütz H. Eur J Clin Pharmacol. 2015 Mar;71(3):271-81. doi: 10.1007/s00228-015-1806-2. Epub 2015 Jan 22. Eur J Clin Pharmacol. 2015. PMID: 25604509 Review.
Assessing goodness-of-fit for evaluation of dose-proportionality.
Wolfsegger MJ, Bauer A, Labes D, Schütz H, Vonk R, Lang B, Lehr S, Jaki TF, Engl W, Hale MD. Wolfsegger MJ, et al. Among authors: schutz h. Pharm Stat. 2021 Mar;20(2):272-281. doi: 10.1002/pst.2074. Epub 2020 Oct 15. Pharm Stat. 2021. PMID: 33063443
Pharmacokinetics of a Modified-Release Dexamphetamine Sulfate Formulation Following Single and Multiple Dosing in Healthy Adults: Comparative Bioavailability with Immediate-Release Dexamphetamine Sulfate, between Strengths, Assessment of Food and Meal Composition Effects.
Sandersleben HU, Mayer A, Ruhmann M, Dangel O, Schütz H. Sandersleben HU, et al. Among authors: schutz h. Scand J Child Adolesc Psychiatr Psychol. 2023 Nov 30;11(1):132-142. doi: 10.2478/sjcapp-2023-0014. eCollection 2023 Jan. Scand J Child Adolesc Psychiatr Psychol. 2023. PMID: 38033826 Free PMC article.
12 results