A Study of Guselkumab in Participants With Crohn's Disease and Ulcerative Colitis
Recruiting now
Conditions studied: Crohn Disease, Colitis, Ulcerative
In brief
The purpose of this study is to evaluate how long a participant keeps taking guselkumab or continues with their treatment plan without stopping (treatment persistence) in participants with moderate to severe Crohn's disease (CD) or ulcerative colitis (UC) in real-world setting. CD and UC are inflammatory bowel diseases, a group of inflammatory conditions of the colon and small intestine.
Key facts
- Study ID
- NCT07606339
- Run by
- Janssen-Cilag Pharma GmbH
- People needed
- 35
- Starts
- 2026-06-10
- Expected to finish
- 2029-06-15
- Last updated by the study team
- 2026-07-31
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Must be eligible for biologic treatment and initiate guselkumab according to the approved indications as described in the current version of the summary of product characteristics (SmPC) of drug. Decision to prescribe must solely be made by the treating physician. Enrolment must take place before or on the day of the first administration
- Confirmed diagnosis of moderate-to-severe UC or CD disease record in their medical records
- Must sign a participation agreement/informed consent form (ICF) allowing source data verification in accordance with local requirements
You may not qualify if…
- Contraindicated to guselkumab per the label
- Is currently enrolled in an interventional clinical study
- Has been previously exposed to interleukin (IL)-23 inhibitors, including Tremfya (guselkumab), Skyrizi (risankizumab) and Omvoh (mirikizumab). As an exception, participants with history of Ustekinumab exposure may be included
- History of more than 4 lines of advanced inflammatory bowel disease (IBD) therapy (biologics and/or small molecules)
- Is unable to provide informed consent
Where it is running
- Medical University Vienna — Vienna, Austria (enrolling)
Full record on ClinicalTrials.gov
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