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dc.rights.licenseopenen_US
hal.structure.identifierImmunology from Concept and Experiments to Translation [ImmunoConcept]
dc.contributor.authorRICHEZ, Christophe
hal.structure.identifierImmunology from Concept and Experiments to Translation [ImmunoConcept]
dc.contributor.authorTRUCHETET, Marie Elise
dc.date.accessioned2022-11-14T13:52:58Z
dc.date.available2022-11-14T13:52:58Z
dc.date.issued2021-08-26
dc.identifier.issn1465-6566 (print) 1744-7666 (online)en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/170253
dc.description.abstractEnIntroduction: Despite the availability of an extensive armamentarium, rheumatoid arthritis (RA) remains a therapeutic challenge for rheumatologists. Janus kinase inhibitors (JAKi) are an emerging class of targeted therapies. The number of JAKi has been growing and to date, filgotinib is the latest JAKi to be approved for use in RA. Areas covered: This review focuses on the pharmacodynamics, pharmacokinetics, efficacy and safety of filgotinib in patients with RA. Expert opinion: Filgotinib is an oral targeted synthetic disease-modifying antirheumatic drug (DMARD) that specifically inhibits JAKi. Filgotinib monotherapy, or a combination regimen with conventional synthetic (cs) DMARDs, has demonstrated efficacy in decreasing disease activity, with a well-managed safety profile in patients with early RA naive to DMARDs, and in RA that does not adequately respond to csDMARDs and/or biologic DMARDs. The selective inhibition of JAK1 may confer an improved safety profile, but further study is required as a potential testicular toxicity has been suggested. Filgotinib offers several advantages: oral administration, rapidity of action, efficacy as monotherapy, and demonstrated activity in difficult to treat RA. However, the placement of filgotinib in the therapeutic arsenal for RA may be influenced by the ongoing collection of long-term safety data from JAKi as a class.
dc.language.isoENen_US
dc.subject.enFilgotinib
dc.subject.enHerpes zoster virus
dc.subject.enJAK1
dc.subject.enMonotherapy
dc.subject.enRheumatoid arthritis
dc.subject.enSpermatogenesis
dc.title.enEvaluating filgotinib for the treatment of rheumatoid arthritis
dc.typeArticle de revueen_US
dc.identifier.doi10.1080/14656566.2021.1967929en_US
dc.subject.halSciences du Vivant [q-bio]/Immunologieen_US
dc.identifier.pubmed34402699en_US
bordeaux.journalExpert Opinion on Pharmacotherapyen_US
bordeaux.page2435–2444en_US
bordeaux.volume22en_US
bordeaux.hal.laboratoriesImmunoConcEpT - UMR 5164en_US
bordeaux.issue18en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03851487
hal.version1
hal.date.transferred2022-11-14T13:53:01Z
hal.exporttrue
dc.rights.ccPas de Licence CCen_US
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