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A comparative study on the efficacy and safety of upadacitinib versus various biologic agents in patients with inflammatory bowel disease

A comparative study on the efficacy and safety of upadacitinib versus various biologic agents in patients with inflammatory bowel disease

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500098001
Enrollment
Unknown
Registered
2025-02-28
Start date
2025-03-01
Completion date
Unknown
Last updated
2025-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inflammatory bowel disease, including ulcerative colitis and Crohn's disease

Interventions

Observation group:None

Sponsors

Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients with a confirmed diagnosis of inflammatory bowel disease. 2.Moderate to severe active inflammatory bowel disease with poor response, intolerance, or contraindications to one or more anti-TNF-a agents. 3.Age >=18 years. 4.Patients voluntarily participate in the study and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1.Concurrent infectious diseases, such as intestinal tuberculosis or infectious colitis. 2.Scheduled inflammatory bowel disease-related surgical treatment within 4 weeks. 3.Concomitant use of other biologic or small molecule agents during the treatment process. 4.Vulnerable populations, including individuals with mental illness, cognitive impairment, critically ill patients, pregnant women, and illiterate individuals.

Design outcomes

Primary

MeasureTime frame
Efficacy;

Secondary

MeasureTime frame
Safety;

Countries

China

Contacts

Public ContactCao Qian

Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University

caoq@srrsh.com+86 571 86006186

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026