Tests tulisokibart in people with moderate to severe Crohn's disease
Tests tulisokibart against placebo in people with active Crohn's disease.
Plain-language title generated from the registry record
Registry title: A Study to Evaluate the Efficacy and Safety of Tulisokibart (MK-7240) in Participants With Moderate to Severe Crohn's Disease (MK-7240-008)
Key facts
- Where
- Berlin, Brandenburg An Der Havel, Duisburg, Hanover, Kiel, Leipzig, Ludwigshafen am Rhein, Lueneburg, Minden, Munich, Pforzheim, Remscheid, Rostock, and Ulm, GermanySee the 15 sites
- Phase
- Phase 3
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 16 and 80 years old?
Source: NCT06430801, who can take part
Where in Germany
- Charite Universitaetsmedizin Berlin KöRBerlin, GermanyNo longer taking part
- Universitaetsklinikum Brandenburg an der Havel GmbHBrandenburg An Der Havel, GermanyNo longer taking part
- Medizinisches Versorgungszentrum fuer spezialaerztliche Versorgung Professor Dr. Friedrichs GmbHDuisburg, GermanyNo longer taking part
- Medizinische Hochschule HannoverHanover, GermanyNo longer taking part
- Universitaetsklinikum Schleswig-Holstein AöRKiel, GermanyNo longer taking part
- Universitaetsklinikum Leipzig AorLeipzig, GermanyNo longer taking part
- St. Marien und St. AnnastiftskrankenhausLudwigshafen am Rhein, GermanyNo longer taking part
- Staedtisches Klinikum Lueneburg gGmbHLueneburg, GermanyNo longer taking part
- Gastroenterologische Gemeinschaftspraxis MindenMinden, GermanyNo longer taking part
- Klinikum der Universitaet Muenchen AöRMunich, GermanyNo longer taking part
- Klinikum rechts der Isar der TU Muenchen AöRMunich, GermanyNo longer taking part
- Siloah St Trudpert KlinikumPforzheim, GermanyNo longer taking part
- Magen-Darm-Zentrum RemscheidRemscheid, GermanyNo longer taking part
- Rostock University Medical CenterRostock, GermanyNo longer taking part
- Universitaetsklinikum Ulm AoRUlm, GermanyNo longer taking part
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?
Trial details
- Who runs it
- Merck Sharp & Dohme LLC
- Trial code
- NCT06430801EU 2023-508636-61-00
- Record updated
- 10 November 2026
- Original description
The purpose of this protocol is to evaluate the efficacy and safety of tulisokibart in participants with moderately to severely active Crohn's disease. Study 1's primary hypotheses are that at least 1 tulisokibart dose level is superior to placebo in the proportion of participants achieving clinical remission per Crohn's Disease Activity Index score (<150, US/FDA) or per stool frequency and abdominal pain score (EU/EMA) and in the proportion of participants achieving endoscopic response at Week 52 (US/FDA and EU/EMA), and that at least 1 tulisokibart dose level is superior to placebo in the proportion of participants achieving clinical remission per Crohn's Disease Activity Index score (<150, US/FDA) or per stool frequency and abdominal pain score (EU/EMA) and in the proportion of participants achieving endoscopic response at Week 12 (US/FDA and EU/EMA). Study 2's primary hypothesis is that at least 1 tulisokibart dose level is superior to placebo in the proportion of participants achieving clinical remission per Crohn's Disease Activity Index score (<150, US/FDA) or stool frequency and abdominal pain score (EU/EMA) and in the proportion of participants achieving endoscopic response at Week 12 (US/FDA and EU/EMA).Read full original descriptionShow less
A Phase 3, Randomized, Double-Blind, Placebo-Controlled Program to Evaluate the Efficacy and Safety of Tulisokibart in Participants With Moderately to Severely Active Crohn's Disease
The purpose of this protocol is to evaluate the efficacy and safety of tulisokibart in participants with moderately to severely active Crohn's disease. Study 1's primary hypotheses are that at least 1 tulisokibart dose level is superior to placebo in the proportion of participants achieving clinical remission per Crohn's Disease Activity Index score (<150, US/FDA) or per stool frequency and abdominal pain score (EU/EMA) and in the proportion of participants achieving endoscopic response at Week 52 (US/FDA and EU/EMA), and that at least 1 tulisokibart dose level is superior to placebo in the proportion of participants achieving clinical remission per Crohn's Disease Activity Index score (<150, US/FDA) or per stool frequency and abdominal pain score (EU/EMA) and in the proportion of participants achieving endoscopic response at Week 12 (US/FDA and EU/EMA). Study 2's primary hypothesis is that at least 1 tulisokibart dose level is superior to placebo in the proportion of participants achieving clinical remission per Crohn's Disease Activity Index score (<150, US/FDA) or stool frequency and abdominal pain score (EU/EMA) and in the proportion of participants achieving endoscopic response at Week 12 (US/FDA and EU/EMA).
Inclusion: Has had a diagnosis of Crohn's disease (CD) at least 3 months before study; Has moderately to severely active CD; Demonstrated inadequate response, loss of response, or intolerance to one or more of the following categories of drugs: oral locally acting steroids, systemic steroids, immunomodulators, biologic and/or small molecule advanced therapies; Adolescent participants ≥16 and <18 years of age can participate if approved by the country or regulatory/health authority.
Exclusion: Currently has any of the following complications of CD: suspected or diagnosed with intra-abdominal or perianal abscess, known symptomatic stricture or colonic stenosis not passable in endoscopy, fulminant colitis, toxic megacolon, or any other manifestation that might require surgery while enrolled in the study; Has surgical bowel resection within 3 months of study; Has prior or current gastrointestinal dysplasia; Prior exposure to tulisokibart (MK-7240, PRA023) or another anti-tumor necrosis factor-like cytokine 1A (TL1A) antibody (Ab); Has been diagnosed with short gut or short bowel syndrome, or any other uncontrolled chronic diarrhea besides CD; Has chronic infection requiring ongoing antimicrobial treatment; Is infected with Hepatitis B virus (HBV), Hepatitis C virus (HCV), or human immunodeficiency virus (HIV); Has active tuberculosis; Has confirmed or suspected coronavirus disease of 2019 (COVID-19) infection; Has a history of cancer (except fully treated non-melanoma skin cell cancers or cervical carcinoma in situ after complete surgical removal) and is disease free for <5 years; Has diagnosis of ulcerative colitis (UC) or indeterminate colitis; Has CD isolated to the stomach, duodenum, jejunum, or perianal region, without colonic and/or ileal involvement; Has current stoma or need for colostomy or ileostomy; Is missing >2 segments of the following 5 segments: terminal ileum, right colon, transverse colon, sigmoid and left colon, and rectum.
The main inclusion and exclusion criteria include but are not limited to the following:.