From:  Therapeutic role of JAK inhibitors in hepatogastrointestinal diseases

 JAK inhibitors with potential use in IBD.

DrugTargetRoute of administration and dosesClinical trial
Tofacitinib [7072]JAK1, 3Oral induction 10 mg BID; maintenance 5 mg BID (may increase to 10 mg BID in non-responders)Phase III trials (OCTAVE Induction 1/2, Sustain, Open; RIVETING); FDA approved for UC
Filgotinib [73]JAK1Oral 200 mg ODPhase III, UC
Upadacitinib [74, 75]JAK1Oral induction 45 mg OD; maintenance 15 mg or 30 mg ODPhase III, FDA approved in 2022 for UC
Izencitinib (TD-1473) [76]JAK 1, 2, 3, TYK2Oral gut specific 270 mg ODPhase I, UC
Peficitinib (Smyraf) [77]JAK 1, 2, 3, TYK2Oral 150 mg ODPhase IIb, UC
Ritlecitinib (Litfulo) [78]JAK3Oral 20 mg, 70 mg, or 200 mg ODPhase II, umbrella study for UC
Brepocitinib [78]TYK2, JAK1Oral 10 mg, 30 mg, or 60 mg ODPhase II, umbrella study for UC
Deucravacitinib (Sotyktu) [79]TYK2Oral 6 mg or 12 mg BIDPhase II, multiple immune-mediated disorders (including preclinical IBD models)
Ivarmacitinib [80]JAK1Oral 4 mg OD, 4 mg BID, or 8 mg ODPhase II, UC

CD: Crohn’s disease; IBD: inflammatory bowel disease; JAK: Janus kinase; TYK2: tyrosine kinase 2; UC: ulcerative colitis. Adapted from [21]. © 2023 by the authors. Distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).