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Selection and Efficacy-Influencing Factors of First-Line Biologic Agents in Moderate-to-Severe Ulcerative Colitis

NCT06962020 · Xijing Hospital of Digestive Diseases
In plain English

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Official title
Selection and Efficacy-Influencing Factors of First-Line Biologic Agents in Moderate-to-Severe Ulcerative Colitis: A Prospective, Multi-Center, Real-World Study
About this study
The purpose of this prospective, multicenter, real-world study is to compare the efficacy differences and influencing factors of different first-line biologics in patients with moderate to severe ulcerative colitis. The question that this study aims to answer is: When treating patients with moderate to severe ulcerative colitis, should IFX or VDZ be prioritized as the first-line choice for biologics?, Which biological agent has better therapeutic effect?. Researchers will observe and follow up with patients with moderate to severe ulcerative colitis treated with different biologics on the front line, evaluate their condition changes, eliminate relevant interfering factors, and draw the final conclusion.
Eligibility criteria
Inclusion Criteria: * Age range of 18-70 years old, gender not limited; * According to international guidelines and consensus, patients with ulcerative colitis should be diagnosed to exclude radiation enteritis, infectious enteritis, tumor related diseases, etc; * Patients assessed as moderate to severe ulcerative colitis based on the Mayo score; * During the follow-up period, no relevant treatments (drugs and surgery) were used that could affect the assessment of the efficacy of biologics Exclusion Criteria: * Patients with hemodynamic instability; * Patients with obvious liver and kidney function injury: bilirubin, aminotransferase (ALT, AST) exceeded the upper limit of normal by 2 times; eGFR\<60ml/min or dialysis patients; * Patients allergic to IFX or VDZ; * Patients whose primary disease was gastrointestinal malignancy; * Patients currently suffering from serious or uncontrolled underlying diseases of the blood, digestive tract, metabolism, endocrine, lung, heart, nervous system, mental system, etc.; * Female patients during pregnancy and breastfeeding (including patients with reproductive needs); * Patients with current infection with infectious diseases (hepatitis B, hepatitis C, syphilis, AIDS, tuberculosis, etc.); * Patients who cannot cooperate with regular follow-up and review of laboratory indicators; * Any other circumstances which, in the opinion of the investigator, would render the subject unfit for study inclusion.
Study design
Enrollment target: 400 participants
Age groups: adult, older_adult
Timeline
Starts: 2025-04-30
Estimated completion: 2025-11-20
Last updated: 2025-07-03
Interventions
Drug: first-line biologic:IFXDrug: first-line biologic:VDZ
Primary outcomes
  • Clinical remission rates and endoscopic remission rates at 14 weeks, 30 weeks, 52 weeks, and 2 years after first-line biologics treatment (From enrollment to the end of treatment at 2 years.)
Sponsor
Xijing Hospital of Digestive Diseases · other
Contacts & investigators
ContactDongdong He · contact · 929731975@qq.com · 0086 + 02984771535
InvestigatorMin Chen · study_director, Xijing Hospital of Digestive Diseases
All locations (1)
Xijing Hospital of Digestive DiseasesRecruiting
Shanxi, Xi'an, China
Selection and Efficacy-Influencing Factors of First-Line Biologic Agents in Moderate-to-Severe Ulcerative Colitis · TrialPath