Critical Remarks on Reference-Scaled Average Bioequivalence von Schütz, Helmut, Labes, Detlew, Wolfsegger, Martin J.

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Distinct characteristics of antibody responses against factor VIII in healthy individuals and in different cohorts of hemophilia A patients von Whelan, Shawn F.J., Hofbauer, Christoph J., Horling, Frank M., Allacher, Peter, Wolfsegger, Martin J., Oldenburg, Johannes, Male, Christoph, Windyga, Jerzy, Tiede, Andreas, Schwarz, Hans Peter, Scheiflinger, Friedrich, Reipert, Birgit M.

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The potential of the estimands framework for clinical pharmacology trials: Some discussion points von Ring, Arne, Wolfsegger, Martin J.

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Assessment of pharmacokinetic linearity after repeated drug administration von Bauer, Alexander, Kagedal, Matts, Wolfsegger, Martin J.

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Recurrent events modelling of haemophilia bleeding events von Titman, Andrew C., Wolfsegger, Martin J., Jaki, Thomas F.

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Non-compartmental estimation of pharmacokinetic parameters for flexible sampling designs von Jaki, Thomas, Wolfsegger, Martin J.

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Estimation in AB/BA crossover trials with application to bioequivalence studies with incomplete and complete data designs von Jaki, Thomas, Pallmann, Philip, Wolfsegger, Martin J.

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Adjustment of endogenous concentrations in pharmacokinetic modeling von Bauer, Alexander, Wolfsegger, Martin J.

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Two-component polyethylene glycol surgical sealant influence on intraperitoneal infection in a refined rodent model von Rodgers, Kathleen E., PhD, Burleson, Florence G., PhD, Burleson, Gary R., PhD, Wolfsegger, Martin J., PhD, Lewis, Kevin M., DVM, Redl, Heinz, PhD

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Authors' reply to Comments on 'Estimation in AB/BA crossover trials with application to bioequivalence studies with incomplete and complete data designs von Jaki, Thomas, Pallmann, Philip, Wolfsegger, Martin J.

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Assessing goodness‐of‐fit for evaluation of dose‐proportionality von Wolfsegger, Martin J., Bauer, Alexander, Labes, Detlew, Schütz, Helmut, Vonk, Richardus, Lang, Benjamin, Lehr, Stephan, Jaki, Thomas F., Engl, Werner, Hale, Michael D.

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hybrid method to estimate the minimum effective dose for monotone and non‐monotone dose–response relationships von Wolfsegger, Martin J, Gutjahr, Georg, Engl, Werner, Jaki, Thomas

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A comparison of methods for classifying samples as truly specific with confirmatory immunoassays von Jaki, Thomas, Lawo, John-Philip, Wolfsegger, Martin J., Allacher, Peter, Horling, Frank

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A formal comparison of different methods for establishing cut points to distinguish positive and negative samples in immunoassays von Jaki, Thomas, Lawo, John-Philip, Wolfsegger, Martin J., Singer, Julia, Allacher, Peter, Horling, Frank

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Non-compartmental estimation of pharmacokinetic parameters in serial sampling designs von Wolfsegger, Martin J., Jaki, Thomas

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A note on statistical analysis of organ weights in non-clinical toxicological studies von Wolfsegger, Martin J., Jaki, Thomas, Dietrich, Barbara, Kunzler, Jackie A., Barker, Kerry

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Establishing bioequivalence in serial sacrifice designs von Wolfsegger, Martin J

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Confidence intervals for ratios of AUCs in the case of serial sampling: a comparison of seven methods von Jaki, Thomas, Wolfsegger, Martin J., Ploner, Meinhard

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Assessing Systemic Drug Exposure in Repeated Dose Toxicity Studies in the Case of Complete and Incomplete Sampling von Wolfsegger, Martin J., Jaki, Thomas

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Establishing Bioequivalence in Complete and Incomplete Data Designs Using AUCs von Jaki, Thomas, Wolfsegger, Martin J., Lawo, John-Philip

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