Phase 2 Crohn's Disease and Colitis Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
Part A (before starting treatment):
- You have been diagnosed with Inflammatory Bowel Disease (IBD)
- Your IBD is currently active, either based on symptoms measured by standard scoring tools, or shown by a stool test result above a certain level
- Your doctor has determined that a medication called risankizumab is an appropriate treatment option for you
- You are at least 18 years old
- You are willing and able to sign a consent form agreeing to take part
- You already have a medical reason to have a camera procedure (endoscopy) of your bowel
Part B (already on treatment):
- You have been diagnosed with Inflammatory Bowel Disease (IBD)
- You have been taking risankizumab for at least 14 weeks
- You are at least 18 years old
- You are willing and able to sign a consent form agreeing to take part
- You already have a medical reason to have a camera procedure (endoscopy) of your bowel
Who may not be able to join:
- You are pregnant or currently breastfeeding
- You are a woman who has not yet gone through menopause and are not using a reliable form of contraception during the study period and for 10 weeks afterward
- You have a medical or mental health condition that affects your ability to fully understand and agree to taking part in the study
- You have previously been treated with a specific type of medication that targets a protein called IL-23 alone (having had a combination IL-23/IL-12 therapy does not automatically exclude you — confirm with trial site)
- You have active Crohn's disease complications outside the gut, such as certain eye or skin conditions, in sensitive locations (Part A only)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: +31(0)503612620
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Determine the safety of risankizumab-800CW in IBD; Blood pressure; Heart rate; Temperature; Investigate the feasibility of using ex vivo FMI to detect risankizumab-800CW; Investigate the feasibility of using FME to detect risankizumab-800CW signals_1; Investigate the feasibility of using FME to detect risankizumab-800CW signals_2; Investigate the feasibility of using FME to detect risankizumab-800CW signals_3; Determining the optimal imaging dose of risankizumab-800CW
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.