Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/219494
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dc.contributor.authorVan Leeuwen, Jolijn-
dc.contributor.authorQuartuccio, Luca-
dc.contributor.authorDraibe, Juliana-
dc.contributor.authorGunnarson, Iva-
dc.contributor.authorSprangers, Ben-
dc.contributor.authorTeng, Y K Onno-
dc.date.accessioned2025-03-06T07:26:28Z-
dc.date.available2025-03-06T07:26:28Z-
dc.date.issued2025-01-01-
dc.identifier.issn1177-8881-
dc.identifier.urihttps://hdl.handle.net/2445/219494-
dc.description.abstractRecently, avacopan has been approved for the treatment of ANCA-associated vasculitis (AAV). Avacopan is an inhibitor of the C5a-receptor, which plays an important role in chemotaxis and the amplification loop of inflammation in AAV. In the most recent, international guidelines avacopan is recommended as steroid-sparing agents for the management of AAV. Here, we review the clinical trials that have led to demonstrate that avacopan is an effective treatment option in the management of AAV, where it can significantly reduce the cumulative dosage of glucocorticoids (GC). Despite the new guideline recommendations, clear guidance on how to employ avacopan in real-world clinical practice is lacking. We therefore also address in this review the data and clinical experience with avacopan obtained from real-world evidence. Combining preclinical studies, clinical trials, and real-world evidence helps to provide a better position of avacopan for the management of AAV in routine clinical practice, taking advantage of the GC-sparing effects of avacopan as a possible solution for the current challenge of reducing GC-toxicity in AAV patients. Furthermore, we delineate current knowledge gaps and future research areas that need to be addressed.-
dc.format.extent15 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherDove Medical Press Limited-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.2147/DDDT.S341842-
dc.relation.ispartofDrug Design, Development and Therapy, 2025, vol. 19, p. 23-37-
dc.relation.urihttps://doi.org/10.2147/DDDT.S341842-
dc.rightscc-by-nc (c) Van Leeuwen, Jolijn et al., 2025-
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))-
dc.subject.classificationVasculitis-
dc.subject.classificationMalalties autoimmunitàries-
dc.subject.classificationTerapèutica-
dc.subject.otherVasculitis-
dc.subject.otherAutoimmune diseases-
dc.subject.otherTherapeutics-
dc.titleEvaluating Avacopan in the Treatment of ANCA-Associated Vasculitis: Design, Development and Positioning of Therapy-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.date.updated2025-02-05T09:37:52Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid39803605-
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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