These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
290 related articles for article (PubMed ID: 25004823)
1. Simulation of monoclonal antibody pharmacokinetics in humans using a minimal physiologically based model. Li L; Gardner I; Dostalek M; Jamei M AAPS J; 2014 Sep; 16(5):1097-109. PubMed ID: 25004823 [TBL] [Abstract][Full Text] [Related]
2. Towards a platform PBPK model to characterize the plasma and tissue disposition of monoclonal antibodies in preclinical species and human. Shah DK; Betts AM J Pharmacokinet Pharmacodyn; 2012 Feb; 39(1):67-86. PubMed ID: 22143261 [TBL] [Abstract][Full Text] [Related]
3. A Minimal Physiologically Based Pharmacokinetic Model with a Nested Endosome Compartment for Novel Engineered Antibodies. Yuan D; Rode F; Cao Y AAPS J; 2018 Mar; 20(3):48. PubMed ID: 29541870 [TBL] [Abstract][Full Text] [Related]
4. Model-Based Assessment of the Contribution of Monocytes and Macrophages to the Pharmacokinetics of Monoclonal Antibodies. Malik PRV; Hamadeh A; Edginton AN Pharm Res; 2022 Feb; 39(2):239-250. PubMed ID: 35118567 [TBL] [Abstract][Full Text] [Related]
5. The interplay of non-specific binding, target-mediated clearance and FcRn interactions on the pharmacokinetics of humanized antibodies. Datta-Mannan A; Lu J; Witcher DR; Leung D; Tang Y; Wroblewski VJ MAbs; 2015; 7(6):1084-93. PubMed ID: 26337808 [TBL] [Abstract][Full Text] [Related]
6. Evaluation of a catenary PBPK model for predicting the in vivo disposition of mAbs engineered for high-affinity binding to FcRn. Chen Y; Balthasar JP AAPS J; 2012 Dec; 14(4):850-9. PubMed ID: 22956476 [TBL] [Abstract][Full Text] [Related]
7. Physiologically-based pharmacokinetic (PBPK) model to predict IgG tissue kinetics in wild-type and FcRn-knockout mice. Garg A; Balthasar JP J Pharmacokinet Pharmacodyn; 2007 Oct; 34(5):687-709. PubMed ID: 17636457 [TBL] [Abstract][Full Text] [Related]
8. A minimal physiologically based pharmacokinetic model to investigate FcRn-mediated monoclonal antibody salvage: Effects of K Maas BM; Cao Y MAbs; 2018; 10(8):1322-1331. PubMed ID: 30130450 [TBL] [Abstract][Full Text] [Related]
9. Combined glyco- and protein-Fc engineering simultaneously enhance cytotoxicity and half-life of a therapeutic antibody. Monnet C; Jorieux S; Souyris N; Zaki O; Jacquet A; Fournier N; Crozet F; de Romeuf C; Bouayadi K; Urbain R; Behrens CK; Mondon P; Fontayne A MAbs; 2014; 6(2):422-36. PubMed ID: 24492301 [TBL] [Abstract][Full Text] [Related]
10. Are endosomal trafficking parameters better targets for improving mAb pharmacokinetics than FcRn binding affinity? Gurbaxani B; Dostalek M; Gardner I Mol Immunol; 2013 Dec; 56(4):660-74. PubMed ID: 23917469 [TBL] [Abstract][Full Text] [Related]
11. Physiologically-based pharmacokinetic modeling to predict the clinical pharmacokinetics of monoclonal antibodies. Glassman PM; Balthasar JP J Pharmacokinet Pharmacodyn; 2016 Aug; 43(4):427-46. PubMed ID: 27377311 [TBL] [Abstract][Full Text] [Related]
12. Incorporation of FcRn-mediated disposition model to describe the population pharmacokinetics of therapeutic monoclonal IgG antibody in clinical patients. Ng CM Biopharm Drug Dispos; 2016 Mar; 37(2):107-19. PubMed ID: 26581439 [TBL] [Abstract][Full Text] [Related]
13. Physiologically based pharmacokinetic (PBPK) model that describes enhanced FcRn-dependent distribution of monoclonal antibodies (mAbs) by pI-engineering in mice. Naoi S; Yamane M; Nemoto T; Kato M; Saito R; Tachibana T Drug Metab Pharmacokinet; 2023 Dec; 53():100506. PubMed ID: 38029470 [TBL] [Abstract][Full Text] [Related]
14. Scale-up of a physiologically-based pharmacokinetic model to predict the disposition of monoclonal antibodies in monkeys. Glassman PM; Chen Y; Balthasar JP J Pharmacokinet Pharmacodyn; 2015 Oct; 42(5):527-40. PubMed ID: 26364301 [TBL] [Abstract][Full Text] [Related]
15. Minimal Physiologically-based Pharmacokinetic Model to Investigate the Effect of Charge on the Pharmacokinetics of Humanized anti-HCV-E2 IgG Antibodies in Sprague-Dawley Rats. Hardiansyah D; Ng CM Pharm Res; 2022 Mar; 39(3):481-496. PubMed ID: 35246757 [TBL] [Abstract][Full Text] [Related]
16. A Physiologically-Based Pharmacokinetic Model for the Prediction of "Half-Life Extension" and "Catch and Release" Monoclonal Antibody Pharmacokinetics. Jones HM; Tolsma J; Zhang Z; Jasper P; Luo H; Weber GL; Wright K; Bard J; Bell R; Messing D; Kelleher K; Piche-Nicholas N; Webster R CPT Pharmacometrics Syst Pharmacol; 2020 Sep; 9(9):534-541. PubMed ID: 32697437 [TBL] [Abstract][Full Text] [Related]
17. A Minimal Physiologically-Based Pharmacokinetic Model Demonstrates Role of the Neonatal Fc Receptor (FcRn) Competition in Drug-Disease Interactions With Antibody Therapy. Abdallah HM; Zhu AZX Clin Pharmacol Ther; 2020 Feb; 107(2):423-434. PubMed ID: 31449666 [TBL] [Abstract][Full Text] [Related]
18. A novel in vitro assay to predict neonatal Fc receptor-mediated human IgG half-life. Souders CA; Nelson SC; Wang Y; Crowley AR; Klempner MS; Thomas W MAbs; 2015; 7(5):912-21. PubMed ID: 26018774 [TBL] [Abstract][Full Text] [Related]
19. Incorporating target-mediated drug disposition in a minimal physiologically-based pharmacokinetic model for monoclonal antibodies. Cao Y; Jusko WJ J Pharmacokinet Pharmacodyn; 2014 Aug; 41(4):375-87. PubMed ID: 25077917 [TBL] [Abstract][Full Text] [Related]
20. Application of Physiologically Based Pharmacokinetic Modeling to Predict the Effects of FcRn Inhibitors in Mice, Rats, and Monkeys. Li T; Balthasar JP J Pharm Sci; 2019 Jan; 108(1):701-713. PubMed ID: 30423340 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]