{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,5,14]],"date-time":"2025-05-14T01:07:07Z","timestamp":1747184827554,"version":"3.40.5"},"reference-count":36,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2024,6,16]],"date-time":"2024-06-16T00:00:00Z","timestamp":1718496000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Fundamemntal Clinical Pharma"],"published-print":{"date-parts":[[2024,10]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>Mycophenolate mofetil (MMF) has been used to treat interstitial lung disease (ILD), but mycophenolate (MPA) pharmacokinetics was not reported for this use. This ancillary study of the EVER\u2010ILD protocol aimed at describing the pharmacokinetic variability of MPA using population modelling in ILD.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>Concentrations of MPA were measured during an 8\u2010h course for 27 ILD patients treated with 1000\u2009mg MMF b.i.d. Absorption, distribution and elimination of MPA were described using population compartment models with first\u2010order transfer and elimination rate constants, while accounting for both absorption peaks using gamma absorption models.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>The pharmacokinetics of MPA was best described using a two\u2010compartment model and two gamma absorption models, model performances of this model were still similar to those of a one gamma absorption model. This pharmacokinetics seemed to be notably influenced by body weight, renal function and inflammatory status. The distribubtion value area under the concentration curve between two administrations of MMF was AUC<jats:sub>12<\/jats:sub>\u2009=\u200952.5\u00a0mg.h\/L in median (interquartile range: 42.2\u201358.0\u00a0mg.h\/L).<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>This is the first study reporting MPA pharmacokinetics in ILD. This pharmacokinetics appears to be similar to other indications and should be further investigated in future studies.<\/jats:p><\/jats:sec>","DOI":"10.1111\/fcp.13021","type":"journal-article","created":{"date-parts":[[2024,6,17]],"date-time":"2024-06-17T04:14:01Z","timestamp":1718597641000},"page":"1008-1016","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Population pharmacokinetics of mycophenolate in patients treated for interstitial lung disease (EVER\u2010ILD study)"],"prefix":"10.1111","volume":"38","author":[{"given":"Yan\u2010Min","family":"Xu","sequence":"first","affiliation":[{"name":"CHRU de Tours Service de Pneumologie et d'Explorations Fonctionnelles Respiratoires  Tours France"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-4020-4545","authenticated-orcid":false,"given":"David","family":"Ternant","sequence":"additional","affiliation":[{"name":"INSERM 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