Taking people in IsraelPhase 2

Testing risankizumab combined with other drugs in Crohn's disease and ulcerative colitis

Tests risankizumab with trosunilimab or ABBV-701 in adults with active Crohn's disease or ulcerative colitis.

Plain-language title generated from the registry record
Registry title: Study of Advanced Therapies for the Treatment of Adult Participants With Moderately to Severely Active Crohn's Disease or Ulcerative Colitis

Key facts

Where: Ashdod, IsraelSee the site
Phase: Phase 2

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults aged 18 to 75 with moderately to severely active Crohn's disease or ulcerative colitis, who have already tried at least 1 other therapy that did not work.

Age: 18 to 75 years
Sex: All sexes can join.
Disease stage: Moderately to severely active Crohn's disease or ulcerative colitis, diagnosed at least 90 days before the start. A scope exam must show inflammation. Crohn's: CDAI score of 220 or more, and SES-CD of 6 or more (4 or more if only the ileum is affected). Ulcerative colitis: modified Mayo Score of 5 to 9 and endoscopic subscore of 2 to 3.
Earlier treatment: Must have had 1 or more therapies for the disease that failed. Cannot have had an investigational drug within 30 days or 5 half-lives (whichever is longer). Cannot have had certain biologic or small-molecule therapies within the time frame set by the study. Cannot have had bowel surgery in the past 3 months.

Main reasons for not taking part

Intolerance to p19 IL-23 inhibitors, including risankizumab
Bowel resection surgery within the past 3 months
Crohn's: more than 3 earlier bowel resections, or small bowel removed with a combined length over 100 cm (3 ft 3 in)
Ulcerative colitis: earlier colectomy (total or subtotal)
Ulcerative colitis: disease limited to less than 10 cm (3.9 in) of the rectum

Read by machine on 9 November 2026.

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

Are you between 18 and 75 years old?

Source: NCT07697456, who can take part

Where in Israel

Assuta Ashdod Medical Center /ID# 280535Ashdod, IsraelTaking people

Questions to ask the study team

How often do I need to come in, and for how long each time?
Are travel costs paid?
Can I keep my own doctor?
What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

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Trial details

Who runs it: AbbVie
Trial code: NCT07697456 EU 2026-525959-86-00
Record updated: 27 October 2026
Original description: Crohn's disease (CD) and Ulcerative colitis (UC) are 2 types of inflammatory bowel diseases which cause long-lasting, severe inflammation (redness, swelling) in the digestive tract. CD can affect any part of the digestive tract causing many different symptoms including belly pain, diarrhea, tiredness, and weight loss. UC affects the lining of the rectum and colon (large intestine) and can cause bleeding, belly pain, and diarrhea. This platform basket study will evaluate how safe and effective advanced therapies are in adults with moderately to severely active Crohn's Disease (CD) or Ulcerative Colitis (UC).Read full original descriptionShow less
A Phase 2 Platform Basket Study Evaluating Advanced Therapies in Subjects With Moderately to Severely Active Crohn's Disease or Ulcerative Colitis
Crohn's disease (CD) and Ulcerative colitis (UC) are 2 types of inflammatory bowel diseases which cause long-lasting, severe inflammation (redness, swelling) in the digestive tract. CD can affect any part of the digestive tract causing many different symptoms including belly pain, diarrhea, tiredness, and weight loss. UC affects the lining of the rectum and colon (large intestine) and can cause bleeding, belly pain, and diarrhea. This platform basket study will evaluate how safe and effective advanced therapies are in adults with moderately to severely active Crohn's Disease (CD) or Ulcerative Colitis (UC).
This study currently includes 2 substudies evaluating different treatments in participants with CD or UC. Substudy 1 will evaluate the combination of risankizumab and trosunilimab (ABBV-466) and Substudy 2 will evaluate the combination of risankizumab and ABBV-701 (ABBV-7066). When adult participants with moderately to severely active CD or UC join the study, they will undergo a 2-step randomization within CD and UC substudies, respectively. The first unblinded randomization will assign participants into a substudy, and the second blinded randomization will assign participants to a treatment arm within the assigned substudy. Approximately 100 adult participants will be enrolled per treatment arm across both substudies at approximately 400 sites worldwide.
There may be higher treatment burden for participants in this trial compared to their standard of care treatment without participating in this study. Participants will attend regular visits during the study at a hospital or clinic. The effect of the treatment will be checked by medical assessments, blood tests, stool tests, endoscopies, checking for side effects and completing questionnaires and a daily diary.
Inclusion: CD specific:; Crohn's Disease Activity Index (CDAI) score of ≥ 220; Confirmed diagnosis of CD at least 90 days prior to Baseline; Endoscopic evidence of mucosal inflammation as documented by an Simple Endoscopic Score for Crohn's Disease (SES-CD) of ≥ 6 for ileocolonic or colonic disease or SES-CD of ≥ 4 for isolated ileal disease; Demonstrated failure of 1 or more therapy for CD; UC specific:; Confirmed diagnosis of UC at least 90 days prior to Baseline; Active UC with a modified Mayo Score (mMS) of 5 to 9 points and endoscopic subscore (ESS) of 2 to 3; Demonstrated failure of 1 or more therapy for UC.
Exclusion: Participants with demonstrated intolerance to p19 IL-23 inhibitors (including risankizumab); Participants treated with any investigational drug within 30 days or 5 half-lives of the study treatments (whichever is longer) prior to the first dose of study treatment; Participants who received any ATs (biologic or small molecules) prior to first dose of study treatment within the protocol specified time frame; Participants with surgical bowel resection within the past 3 months prior to Baseline; CD specific:; Participants with >3 prior bowel resections; Participants with previous small bowel resection(s) of combined length >100 cm; UC specific:; Participants with prior colectomy (total or subtotal); Participants with extent of disease limited to < 10 cm of rectum.
ClinicalTrials.gov NCT07697456 · EU CTIS 2026-525959-86-00