Model-Informed Precision Dosing during Infliximab Induction Therapy Reduces Variability in Exposure and Endoscopic Improvement between Patients with Ulcerative Colitis.

endoscopy inflammatory bowel disease infliximab model-informed precision dosing monoclonal antibody population pharmacokinetics-pharmacodynamics simulations therapeutic drug monitoring ulcerative colitis

Journal

Pharmaceutics
ISSN: 1999-4923
Titre abrégé: Pharmaceutics
Pays: Switzerland
ID NLM: 101534003

Informations de publication

Date de publication:
06 Oct 2021
Historique:
received: 27 08 2021
revised: 24 09 2021
accepted: 27 09 2021
entrez: 23 10 2021
pubmed: 24 10 2021
medline: 24 10 2021
Statut: epublish

Résumé

Model-informed precision dosing (MIPD) may be a solution to therapeutic failure of infliximab for patients with ulcerative colitis (UC), as underexposure could be avoided, and the probability of endoscopic improvement (pEI; Mayo endoscopic subscore ≤ 1) could be optimized. To investigate in silico whether this claim has merit, four induction dosing regimens were simulated: 5 mg/kg (label dosing), 10 mg/kg, covariate-based MIPD (fat-free mass, corticosteroid use, and presence of extensive colitis at baseline), and concentration-based MIPD (based on the trough concentration at day 14). Covariate- and concentration-based MIPD were chosen to target the same median area under the infliximab concentration-time curve up to endoscopy at day 84 (AUC

Identifiants

pubmed: 34683916
pii: pharmaceutics13101623
doi: 10.3390/pharmaceutics13101623
pmc: PMC8537637
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Fonds Wetenschappelijk Onderzoek
ID : T.B. received a TBM grant (grant number T003117N)
Organisme : Fonds Wetenschappelijk Onderzoek
ID : P.D. received a TBM grant (grant number T003716N)
Organisme : Fonds Wetenschappelijk Onderzoek
ID : M.F. is a Senior Clinical Investigator
Organisme : Fonds Wetenschappelijk Onderzoek
ID : E.D. is a postdoctoral research fellow (grant number: 12X9420N)

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Auteurs

Ruben Faelens (R)

Department of Pharmaceutical and Pharmacological Sciences, Katholieke Universiteit Leuven, 3000 Leuven, Belgium.

Zhigang Wang (Z)

Department of Pharmaceutical and Pharmacological Sciences, Katholieke Universiteit Leuven, 3000 Leuven, Belgium.

Thomas Bouillon (T)

Department of Pharmaceutical and Pharmacological Sciences, Katholieke Universiteit Leuven, 3000 Leuven, Belgium.

Paul Declerck (P)

Department of Pharmaceutical and Pharmacological Sciences, Katholieke Universiteit Leuven, 3000 Leuven, Belgium.

Marc Ferrante (M)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, 3000 Leuven, Belgium.
Department of Chronic Diseases and Metabolism, Katholieke Universiteit Leuven, 3000 Leuven, Belgium.

Séverine Vermeire (S)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, 3000 Leuven, Belgium.
Department of Chronic Diseases and Metabolism, Katholieke Universiteit Leuven, 3000 Leuven, Belgium.

Erwin Dreesen (E)

Department of Pharmaceutical and Pharmacological Sciences, Katholieke Universiteit Leuven, 3000 Leuven, Belgium.

Classifications MeSH