JAK1 inhibition and inflammatory bowel disease

Abstract Primary non-response and secondary loss of response remain a significant issue with the currently available treatment options for a significant proportion of patients with inflammatory bowel disease (IBD). There are multiple unmet needs in the IBD treatment algorithm and new treatment optio...

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Veröffentlicht in:Rheumatology (Oxford, England) England), 2021-05, Vol.60 (Supplement_2), p.ii45-ii51
Hauptverfasser: Harris, Clare, Cummings, J R Fraser
Format: Artikel
Sprache:eng
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Zusammenfassung:Abstract Primary non-response and secondary loss of response remain a significant issue with the currently available treatment options for a significant proportion of patients with inflammatory bowel disease (IBD). There are multiple unmet needs in the IBD treatment algorithm and new treatment options are required. As our understanding of the pathogenesis of IBD evolves, new therapeutic targets are being identified. The JAK-STAT pathway has been extensively studied. Tofacitinib, a JAK1 inhibitor, is now licensed for use in the induction and maintenance of ulcerative colitis and there are a large number of molecules currently under investigation. These new small molecule drugs (SMDs) will challenge current treatment pathways at a time when clinical therapeutic outcomes are rapidly evolving and becoming more ambitious. This is a review of the current JAK1 inhibitors in IBD including the current evidence from clinical trials.
ISSN:1462-0324
1462-0332
1462-0332
DOI:10.1093/rheumatology/keaa896