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Study identifier: NCT07550673 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Upadacitinib Versus Infliximab as Second-Line Treatment for Acute Severe Ulcerative Colitis(UPRISE)

Condition: Acute Severe Ulcerative Colitis  ·  Sponsor: Xijing Hospital of Digestive Diseases

PhasePhase 4
Planned participants226
Who can joinAll sexes, 18 Years to 85 Years
Healthy volunteersNo

About this study

This clinical trial aims to evaluate the comparative efficacy and safety of upadacitinib versus infliximab as second-line treatments for acute severe ulcerative colitis, addressing the following key questions: (1) Can upadacitinib as a second-line therapy effectively induce remission in acute severe ulcerative colitis with efficacy non-inferior to infliximab? (2) What adverse reactions may occur with upadacitinib in the treatment of acute severe ulcerative colitis? Researchers will also compare the efficacy of upadacitinib with that of corticosteroids to assess its therapeutic effect. Participants will be assigned to either the upadacitinib group (receiving upadacitinib extended-release tablets 45 mg once daily for 8 weeks, followed by 30 mg once daily) or the infliximab group (receiving an initial dose of 5 mg/kg, with additional doses at week 2, week 6, and every 8 weeks thereafter at the same dose). The treatment duration is 3 months, with outpatient visits for examinations and tests every two weeks. Patients will record their bowel movements and symptoms such as abdominal pain, and undergo colonoscopy, ultrasound examinations, and blood tests at specified time points.

This description comes directly from the study's public registry record.

Talk to the study team

Yongquan Shi, Ph.D  ·  86-029-84771535  ·  shiyquan@fmmu.edu.cn

Always discuss trial participation with your own doctor first.

Locations (4)

Ankang Central HospitalAnkang, Shaanxi, ChinaRecruiting
3201 HospitalHanzhong, Shaanxi, ChinaRecruiting
Xijing Hosipital of Digestive DiseaseXi'an, Shaanxi, ChinaRecruiting
Shaanxi Provincial Nuclear Industry 215 HospitalXianyang, Shaanxi, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07550673