Publications

Tumor necrosis factor-mediated disposition of infliximab in ulcerative colitis patients

Berends S.E., Steeg T.J.v., Ahsman M.J., Singh S,. Brandse J.F., D’Haens G.R.A.M., Mathôt R.A.A. Tumor necrosis factor-mediated disposition of infliximab in ulcerative colitis patients. J. Pharmacokinet. Pharmacodyn.: 5, 2019. [Link to publication]

Favorable Pharmacokinetic Characteristics of Extended ‑ Half ‑ Life Recombinant Factor VIII BAY 94 ‑ 9027

Solms A., Iorio A., Ahsman M. J., Vis P., Shah A., Berntorp E., Garmann D. Favorable Pharmacokinetic Characteristics of Extended ‑ Half ‑ Life Recombinant Factor VIII BAY 94 ‑ 9027 Enable Robust Individual Profiling Using a Population Pharmacokinetic Approach. Clin. Pharmacokinet, 2019. [Link to publication]

Population Pharmacokinetic and Exposure–Response Analysis of Finerenone

Snelder N., Heinig R., Drenth H.J., Joseph A., Kolkhof P., Lippert J., Garmann D., Ploeger B., Eissing T. Population Pharmacokinetic and Exposure–Response Analysis of Finerenone: Insights Based on Phase IIb Data and Simulations to Support Dose Selection for Pivotal Trials in Type 2 Diabetes with Chronic Kidney Disease. Clin. Pharmacokinet: 1179-1926, 2019. [Link to publication]

An integrated population pharmacokinetic analysis to characterize levonorgestrel pharmacokinetics after different administration routes

Reinecke I., Hofmann B., Mesic E., Drenth H.J., Garmann D. An integrated population pharmacokinetic analysis to characterize levonorgestrel pharmacokinetics after different administration routes. J Clin Pharmacol: 1639-1654, 2018. [Link to publication] 

Linear pharmacokinetic parameters for monoclonal antibodies are similar within a species and across different pharmacological targets

Betts A., Keunecke A., Steeg T.J.v., Graaf P.H.v.d., Avery L.B., Jones H., Berkhout J. Linear pharmacokinetic parameters for monoclonal antibodies are similar within a species and across different pharmacological targets: A comparison between human, cynomolgus monkey and hFcRn Tg32 transgenic mouse using a population-modeling approach. MAbs: 1–55, 2018. [Link to publication]

A Perspective on the State of Pharmacometrics and Systems Pharmacology Integration

Trame M.N., Riggs M., Biliouris K., Marathe D., Mettetal J., Post T.M., Rizk M.L., Visser S.A.G., Musante C.J. A Perspective on the State of Pharmacometrics and Systems Pharmacology Integration. CPT Pharmacometrics Syst Pharmacol: 617-620, 2018. [Link to publication] 

Extending a systems model of the APP pathway

Maanen E.M.T.v., Steeg T.J.v., Ahsman M., Michener M.S., Savage M.J., Kennedy M.E., Kleijn H.J., Stone J., Danhof M. Extending a systems model of the APP pathway: Separation of β- and γ-secretase sequential cleavage steps of APP. J. Pharmacol. Exp. Ther.: 507-518, 2018. [Link to publication]

Pharmacokinetic and Pharmacodynamic Modelling to Characterize the Tolerability of Alternative Up-Titration Regimens of Roflumilast in Patients with Chronic Obstructive Pulmonary Disease

Facius A., Marostica E., Gardiner P., Watz H., Lahu G. Pharmacokinetic and Pharmacodynamic Modelling to Characterize the Tolerability of Alternative Up-Titration Regimens of Roflumilast in Patients with Chronic Obstructive Pulmonary Disease. Clin. Pharmacokinet: 1029-1038, 2018. [Link to publication]

Frequency-Domain Response Analysis for Quantitative Systems Pharmacology Models

Schulthess P., Post T.M., Yates J., Graaf P.H.v.d. Frequency-Domain Response Analysis for Quantitative Systems Pharmacology Models. CPT Pharmacometrics Syst Pharmacol: 111–123, 2018. [Link to publication]

Influence of Body Composition on Disposition of the Highly Fat Distributed Compound as Analyzed by Physiologically-based Pharmacokinetic (PBPK) Modeling and Simulation

Goto, A., Tagawa, Y., Moriya, Y., Sato, S., Yamamoto, M., Wakabayashi T., Tsukamoto T., Jongh J.d., Steeg T.J.v., Moriwaki T., Asahi, S. Influence of Body Composition on Disposition of the Highly Fat Distributed Compound as Analyzed by Physiologically-based Pharmacokinetic (PBPK) Modeling and Simulation. Biopharmaceutics & Drug Disposition: 543-552, 2017. [Link to publication]