Skip to content
Study details
Enrolling now

A Study to Assess the Change in Disease Activity in Adult Participants With Moderate to Severe Ulcerative Colitis Treated With Risankizumab Compared to Vedolizumab

AbbVie
NCT IDNCT06880744ClinicalTrials.gov data as of Apr 2026
Phase

Phase 3

Target enrollment

530

Study length

about 3.3 years

Ages

18–80

Locations

74 sites in AL, AZ, CA +24

What this study is about

Researchers are testing whether risankizumab or vedolizumab are effective treatments for adults with moderate to severe ulcerative colitis who haven't received targeted therapies before. The trial will last about 69 weeks, and participants will receive either risankizumab (IV then subcutaneous) or vedolizumab (IV throughout).

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Risankizumab
  • 2.Take Vedolizumab

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IVInjection / IV

How treatment is administered

Treatment Assignment
Randomized (Open Label)

You are randomly assigned, but you will know your treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

risankizumab, vedolizumab

Drug routes

injection, intravenous

Body systems

Gastroenterology