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dc.contributor.authorMarquez-Megias, Silvia-
dc.contributor.authornalda-molina, Ricardo-
dc.contributor.authorMás-Serrano, Patricio-
dc.contributor.authorRamon-Lopez, Amelia-
dc.contributor.otherDepartamentos de la UMH::Ingenieríaes_ES
dc.date.accessioned2025-01-16T12:50:04Z-
dc.date.available2025-01-16T12:50:04Z-
dc.date.created2023-10-
dc.identifier.citationBiomedicines 2023, 11, 2822es_ES
dc.identifier.issn2227-9059-
dc.identifier.urihttps://hdl.handle.net/11000/34576-
dc.description.abstract: Adalimumab is a fully human monoclonal antibody used for the treatment of inflammatory bowel disease (IBD). Due to its considerably variable pharmacokinetics and the risk of developing antibodies against adalimumab, it is highly recommended to use a model-informed precision dosing approach. The aim of this study is to develop a population pharmacokinetic (PopPK) model of adalimumab for patients with IBD based on a literature model (reference model) to be used in the clinical setting. A retrospective observational study with 54 IBD patients was used to develop two different PopPK models based on the reference model. One of the developed models estimated the pharmacokinetic population parameters (estimated model), and the other model incorporated informative priors (prior model). The models were evaluated with bias and imprecision. Clinical impact was also assessed, evaluating the differences in dose interventions. The developed models Citation: Marquez-Megias, S.; Nalda-Molina, R.; Más-Serrano, P.; Ramon-Lopez, A. Population Pharmacokinetic Model of Adalimumab Based on Prior Information Using Real World Data. Biomedicines 2023, 11, 2822. https://doi.org/10.3390/ biomedicines11102822 Academic Editors: Xiaoyu Yan and Giovanni Pallio Received: 20 July 2023 Revised: 14 September 2023 Accepted: 13 October 2023 Published: 18 October 2023 Copyright: © 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/). included the albumin as a continuous covariate on apparent clearance. The prior model was superior to the estimated model in terms of bias, imprecision and clinical impact on the target population. In conclusion, the prior model adequately characterized adalimumab PK in the studied population and was better than the reference model in terms of predictive performance and clinical impactes_ES
dc.formatapplication/pdfes_ES
dc.format.extent12es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectpharmacokineticses_ES
dc.subjectdrug monitoringes_ES
dc.subjectadalimumabes_ES
dc.subjectmonoclonal antibodieses_ES
dc.subjectinflammatory bowel diseaseses_ES
dc.subjectCrohn’s diseasees_ES
dc.subjectulcerative colitises_ES
dc.subject.otherCDU::6 - Ciencias aplicadas::62 - Ingeniería. Tecnologíaes_ES
dc.titlePopulation Pharmacokinetic Model of Adalimumab Based on Prior Information Using Real World Dataes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherversionhttps://doi.org/10.3390/ biomedicines11102822es_ES
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