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DOI 10.1111/jgh.70634

Медицинская библиотека · Journal of gastroenterology and hepatology · 2026

Efficacy, Safety, and Pharmacokinetics of Upadacitinib Among Patients in East Asia With Moderately to Severely Active Ulcerative Colitis: A Post Hoc Subanalysis of Randomized Phase 3 Studies.

Wei Shu Chen, Nakase Hiroshi, Ye Byong Duk, Chao Kang, Wu Hsin-Yun, Eccleston Jason, Yao Xuan, Palac Hannah, Mohamed Mohamed-Eslam F, Ponce-Bobadilla Ana Victoria, Suravaram Smitha, Barrachina Elena Marced, Hisamatsu Tadakazu, Gao Xiang

СтатьяМногоцентровое исследованиеКлиническое исследование III фазыРандомизированное исследованиеПеревод в очереди

Аннотация

BACKGROUND AND AIM: Upadacitinib, a selective Janus kinase 1 inhibitor, is approved to treat moderately to severely active ulcerative colitis (UC). This post hoc subanalysis evaluated the efficacy, safety, and pharmacokinetics of upadacitinib in patients in East Asia.

METHODS

U-ACHIEVE (UC1; NCT02819635) and U-ACCOMPLISH (UC2; NCT03653026) were Phase 3, multicenter, randomized, double-blind, induction studies evaluating upadacitinib 45 mg or placebo daily in adults with moderately to severely active UC. Clinical responders to 8 weeks of upadacitinib induction were eligible to receive upadacitinib 15 mg, upadacitinib 30 mg, or placebo daily in the 52-week U-ACHIEVE maintenance study (UC3; NCT02819635). Efficacy outcomes, safety, and pharmacokinetics were evaluated among East Asian patients.

RESULTS

A higher proportion of East Asian patients achieved clinical remission with upadacitinib than placebo at induction Week 8 (UC1: n = 127, 31.4% vs. 7.3%; UC2: n = 114, 31.2% vs. 2.7%) and maintenance Week 52 (UC3: n = 184, upadacitinib 15 mg, 52.4%; upadacitinib 30 mg, 53.8%; placebo, 10.7%). Rates of endoscopic outcomes were higher with upadacitinib than with placebo across studies. No new safety signals were identified. Herpes zoster occurrences were low (UC1 and UC2: upadacitinib 45 mg, two events [in one patient]; placebo, zero events; UC3: upadacitinib 15 mg, five events; upadacitinib 30 mg, eight events; placebo, zero events). Pharmacokinetics and trends in the relationship between upadacitinib exposure and efficacy were consistent in the East Asian and global populations.

CONCLUSION

Upadacitinib was generally well tolerated and effective for treating moderately to severely active UC in patients in East Asia, with a favorable benefit-risk profile consistent with the global population.

TRIAL REGISTRATION: ClinicalTrials.gov identifier: NCT02819635, NCT03653026.

Для цитирования: Wei Shu Chen, Nakase Hiroshi, Ye Byong Duk, Chao Kang, Wu Hsin-Yun, Eccleston Jason, Yao Xuan, Palac Hannah, Mohamed Mohamed-Eslam F, Ponce-Bobadilla Ana Victoria, Suravaram Smitha, Barrachina Elena Marced, Hisamatsu Tadakazu, Gao Xiang. Efficacy, Safety, and Pharmacokinetics of Upadacitinib Among Patients in East Asia With Moderately to Severely Active Ulcerative Colitis: A Post Hoc Subanalysis of Randomized Phase 3 Studies.. Journal of gastroenterology and hepatology. 2026. DOI: 10.1111/jgh.70634.

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