©The Author(s) 2026.
World J Gastrointest Pharmacol Ther. Mar 5, 2026; 17(1): 112788
Published online Mar 5, 2026. doi: 10.4292/wjgpt.v17.i1.112788
Published online Mar 5, 2026. doi: 10.4292/wjgpt.v17.i1.112788
Table 5 Janus kinase inhibitors in Crohn’s disease
| Drugs | Induction of remission | Induction rates | Long term outcome | Adverse events |
| Tofacitinib[55] | 180 | At 8 weeks clinical remission: 43.5% and 43% with 5 mg and 10 mg group | At 26 weeks, clinical response was maintained in 55.8% and 39.5% patients in 5 mg and 10 mg group respectively | Severe adverse events at 26 weeks 11.7% in 5 mg group and 9.8% in 10 mg group |
| Upadacitinib, Friedberg et al[58] | 40 | At 4 weeks clinical response: 60%; clinical remission: 87% | At 8 weeks clinical response 76%; clinical remission: 70.6% | Acne (23%) |
| Loftus et al[60], U-EXCEL, U-EXCEED and U-ENDURE | U-EXCEL: 526; U-EXCEED: 495; U-ENDURE: 502 | At 12 weeks clinical response was seen in U-EXCEL: 49.5% (vs 29.1% in placebo); U-EXCEED: 38.9% (vs 21.1% in placebo) | At 52 weeks higher patients on upadacitinib had clinical remission vs placebo (15 mg OD: 37.3%; 30 mg OD: 47.6%, 7.3% in placebo) | Herpes zoster; 30 mg group: 7.2 events per 100 person year; 15 mg group: 4.0 events per 100 person year; gastrointestinal perforation: 0.6-0.9 events per 100 person-year |
| Upadacitinib[61] | CELEST: 220; CELEST OLE: 107 | At 12 weeks CLE: Clinical remission: 44.4%; endoscopic response: 40.2% | CELEST OLE: At 52 weeks; clinical: 15 mg: 37.3%; 30 mg: 47.6%; endoscopic: 35.5% with 10 mg/day; 40.1%; remission: 15 mg/day: 19.1%; 30 mg/day: 28.6% | Herpes zoster: 4% in 10 mg group; and 7.2% in 15 mg group |
- Citation: Malakar S, Giri S, Jena A, Nath P. Updated review of Janus kinase inhibitors for the management of inflammatory bowel disease. World J Gastrointest Pharmacol Ther 2026; 17(1): 112788
- URL: https://www.wjgnet.com/2150-5349/full/v17/i1/112788.htm
- DOI: https://dx.doi.org/10.4292/wjgpt.v17.i1.112788