{ "data": { "asOf": "2026-10-30T22:26:31.329Z", "dedupMethod": "exact cross-registry identifier matching; probabilistic = review only", "byRegistry": { "clinicaltrials_gov": 1 }, "canonicalTrial": { "canonicalId": "NCT06095128", "title": "A Study of Vedolizumab With Tofacitinib in Adults With Ulcerative Colitis (UC)", "scientificTitle": "An Open-Label, Phase 4, Single-Arm, Multicenter Study to Evaluate the Induction of Response and Remission of Vedolizumab Dual Targeted Therapy With Tofacitinib in Adult Patients With Moderately to Severely Active Ulcerative Colitis", "status": "active", "studyType": "interventional", "phase": [ "PHASE4" ], "conditions": [ "Ulcerative Colitis" ], "interventions": [ { "name": "Vedolizumab", "type": "DRUG", "description": "Vedolizumab IV infusions" }, { "name": "Tofacitinib", "type": "DRUG", "description": "Tofacitinib Tablets" } ], "sponsor": { "name": "Takeda", "type": "INDUSTRY" }, "locations": [ { "city": "Dothan", "country": "United States", "facility": "Digestive Health Specialsits" }, { "city": "Sun City", "country": "United States", "facility": "GI Alliance Sun City" }, { "city": "Los Angeles", "country": "United States", "facility": "Cedars-Sinai Medical Center" }, { "city": "Newport Beach", "country": "United States", "facility": "Hoag Hospital Newport Beach" }, { "city": "Orlando", "country": "United States", "facility": "Endoscopic Research Inc" }, { "city": "Tampa", "country": "United States", "facility": "Alliance Clinical Research of Tampa, LLC" }, { "city": "Roswell", "country": "United States", "facility": "Gastroenterology Consultants, P.C." }, { "city": "Chicago", "country": "United States", "facility": "University of Chicago Medicine" }, { "city": "Kansas City", "country": "United States", "facility": "University of Kansas Medical Center" }, { "city": "Louisville", "country": "United States", "facility": "University of Louisville" }, { "city": "Metairie", "country": "United States", "facility": "GI Alliance" }, { "city": "New Orleans", "country": "United States", "facility": "Tulane University" }, { "city": "Chevy Chase", "country": "United States", "facility": "Capital Digestive Care - MGG Group - Chevy Chase Clinical Research" }, { "city": "Ypsilanti", "country": "United States", "facility": "Huron Gastroenterology Associates, P.C." }, { "city": "Plymouth", "country": "United States", "facility": "MNGI Digestive Health, PA" }, { "city": "Kansas City", "country": "United States", "facility": "Mid-America Gastro-Intestinal Consultants" }, { "city": "Liberty", "country": "United States", "facility": "BVL Clinical Research" }, { "city": "St Louis", "country": "United States", "facility": "Washington University School of Medicine" }, { "city": "New York", "country": "United States", "facility": "NYU Langone Health" }, { "city": "New York", "country": "United States", "facility": "Weill Cornell Medical College- New York Presbyterian Hospital" }, { "city": "Asheville", "country": "United States", "facility": "Digestive Health Partners" }, { "city": "Chapel Hill", "country": "United States", "facility": "University of North Carolina" }, { "city": "Cincinnati", "country": "United States", "facility": "University of Cincinnati" }, { "city": "Columbus", "country": "United States", "facility": "Ohio Gastroenterology group, Inc." }, { "city": "Westlake", "country": "United States", "facility": "Gastro Intestinal Research Institute of Northern Ohio, LLC." }, { "city": "Wexford", "country": "United States", "facility": "Allegheny Health Network" }, { "city": "Providence", "country": "United States", "facility": "University Gastroenterology" }, { "city": "Rapid City", "country": "United States", "facility": "Sanford Health Research" }, { "city": "Houston", "country": "United States", "facility": "The University of Texas Health Science Center at Houston" }, { "city": "Mansfield", "country": "United States", "facility": "GI Alliance - Mansfield" }, { "city": "San Antonio", "country": "United States", "facility": "Gastroenterology Research of San Antonio, LLC" }, { "city": "Southlake", "country": "United States", "facility": "Texas Digestive Disease Consultants (TDDC), Southlake" }, { "city": "Tyler", "country": "United States", "facility": "Tyler Research Institute, LLC" }, { "city": "Webster", "country": "United States", "facility": "GI Alliance - Webster" }, { "city": "Salt Lake City", "country": "United States", "facility": "University of Utah Health" }, { "city": "Tacoma", "country": "United States", "facility": "Washington Gastroenterology- GIA" }, { "city": "Barrie", "country": "Canada", "facility": "Barrie GI Associates Inc." }, { "city": "London", "country": "Canada", "facility": "London Health Sciences Centre" }, { "city": "Mississauga", "country": "Canada", "facility": "West GTA Endoscopy Inc." }, { "city": "North Bay", "country": "Canada", "facility": "Viable Clinical Research - North Bay" }, { "city": "North York", "country": "Canada", "facility": "Toronto Immune and Digestive Health Institute Inc. (TIDHI)" }, { "city": "Oakville", "country": "Canada", "facility": "ABP Research Services Corp." }, { "city": "Oshawa", "country": "Canada", "facility": "Taunton Surgical Centre" }, { "city": "Vaughan", "country": "Canada", "facility": "Toronto Digestive Disease Associates (TDDA) Inc." }, { "city": "Montreal", "country": "Canada", "facility": "The Research Institute of the McGill University Health Centre" } ], "outcomes": { "other": [], "primary": [ "Percentage of Participants Achieving Clinical Remission at Week 8 Based on Complete Mayo Score" ], "secondary": [ "Percentage of Participants Achieving Clinical Remission at Week 52 Based on Complete Mayo Score", "Percentage of Participants Achieving Clinical Remission at Weeks 8, 14, and 26 Based on Partial Mayo Score", "Percentage of Participants Achieving Clinical Response at Weeks 2, 6, 8, 14, 26 and 52 Based on Complete or Partial Mayo Score", "Percentage of Participants Achieving Clinical Remission at Week 8 and Week 52 Based on Modified Mayo Score", "Percentage of Participants With Endoscopic Improvement at Week 8 and Week 52 Based on Modified Mayo Endoscopic Subscore (MMES)", "Percentage of Participants With Durable Clinical Remission at Week 8 and Week 52", "Percentage of Participants Using Oral Corticosteroids at Baseline Achieving Clinical Remission at Week 8", "Percentage of Participants With Corticosteroid-Free Clinical Remission at Week 8", "Percentage of Participants Using Oral Corticosteroids at Baseline Achieving Clinical Remission at Week 52", "Percentage of Participants With Corticosteroid-Free Clinical Remission at Week 52", "Percentage of Participants Achieving Clinical Response at Week 8", "Percentage of Participants With Endoscopic Improvement at Week 52", "Percentage of Participants With Histological Remission Based on Geboes Score at Week 52", "Change in C-Reactive Protein Levels (CRP) From Baseline", "Change in Fecal Calprotectin Concentrations From Baseline", "Change in Inflammatory Bowel Disease Questionnaire (IBDQ) Score From Baseline", "Change in Functional Assessment of Chronic Illness Therapy Fatigue (FACIT-F) Score From Baseline", "Number of Participants With Adverse Events (AEs), Adverse Events of Special Interest (AESIs) and Serious Adverse Events (SAEs)", "Number of Participants With Clinically Significant Change in Vital Signs From Baseline", "Number of Participants With Clinically Significant Physical Examination Findings", "Number of Participants With Markedly Abnormal Laboratory Values" ] }, "eligibility": { "sex": "ALL", "criteria": "Inclusion Criteria:\n\n1. Has a confirmed diagnosis of UC established at least 3 months prior to screening, by clinical and endoscopic evidence and corroborated by a histopathology report.\n2. Has moderately to severely active UC as determined by a complete Mayo score \\[including PGA\\] of 6 to 12 with a rectal bleeding subscore ≥1 and a centrally assessed endoscopic subscore ≥2 at screening.\n3. Has evidence of UC extending proximally to the rectum \\[≥15 centimeter (cm) of involved colon\\].\n4. Participants with extensive colitis or pancolitis of \\>8 years duration or left sided colitis \\>12 years duration must have documented evidence that a surveillance colonoscopy was performed within 12 months of the initial screening visit.\n5. Participants with a family history of colorectal cancer, personal history of increased colorectal cancer risk, age \\>50 years, or other known risk factors must be up to date on colorectal cancer surveillance.\n6. Has demonstrated an inadequate response to, loss of response to, or intolerance to at least 1, but no more than 2 TNFα antagonists. Determination of inadequate response, loss of response, or intolerance is based upon investigator's clinical judgment. Participants who discontinued TNFα antagonist therapy for reasons other than failure or intolerance (eg, pregnancy) may be eligible after discussion with the medical monitor.\n\nNote: After the interim analysis, participants with inadequate response, loss of response, or intolerance to conventional UC therapy per standard of care treatment without prior exposure to biologics may be enrolled if deemed appropriate. Determination of inadequate response, loss of response, or intolerance is based upon investigator's clinical judgment. Participants who discontinued biologics for reasons other than failure or intolerance (eg, pregnancy) may be eligible after discussion with the Medical Monitor. If using corticosteroids must be on a stable dose of oral corticosteroids up to a maximum of 40 mg daily of prednisone or 9 mg daily of budesonide, or equivalent for at least 2 weeks prior to screening endoscopy and must be willing to follow a mandatory taper of corticosteroids.\n\nExclusion Criteria:\n\nGastrointestinal Exclusion criteria:\n\n1. Has any of the following UC-related complications:\n\n 1. Acute severe UC.\n 2. The participant has had extensive colonic resection, subtotal or total colectomy.\n 3. The participant has clinical evidence of abdominal abscess or toxic megacolon.\n 4. The participant has an ileostomy, colostomy, or known fixed symptomatic stenosis of the intestine.\n 5. Short bowel syndrome.\n2. Has Crohn's colitis, indeterminate colitis, ischemic colitis, nonsteroidal anti-inflammatory drug (NSAID) induced colitis, idiopathic colitis (i.e, colitis not consistent with UC), radiation colitis, microscopic colitis, colonic mucosal dysplasia, or untreated bile acid malabsorption. Participants with a history of colonic mucosal dysplasia are also excluded.\n3. Has uncontrolled primary sclerosing cholangitis.\n\nInfectious Disease Exclusion Criteria:\n\n1. Has any evidence of an active systemic infection during screening. Participants with nonsystemic infections (eg, active fungal infection of nail beds) may be eligible, if in the opinion of the investigator, inclusion of the participant will not interfere with the collection or interpretation of study results and poses no risk to the participant.\n2. Has active or latent tuberculosis (TB), regardless of treatment history, as evidenced by any of the following:\n\n 1. History of TB.\n 2. A diagnostic TB test performed during screening that is positive, as defined by:\n\n i. A positive QuantiFERON test or 2 successive indeterminate QuantiFERON tests or ii. A tuberculin skin test reaction ≥10 mm (≥5 mm in participants receiving the equivalent of \\>15 mg daily prednisone).\n3. A positive test for hepatitis B virus (HBV).\n4. A positive test for hepatitis C virus (HCV).\n5. Evidence of, or treatment for, Clostridium difficile infection or other intestinal pathogen during screening. Participants who test positive for C. difficile or other intestinal pathogens at screening and receive treatment may be enrolled or rescreened (if required) following confirmation of infection resolution.\n6. Evidence of active Cytomegalovirus (CMV) infection at screening.\n\nMedication exclusion criteria:\n\n1. Has received immunomodulators (eg, 6-mercaptopurine, azathioprine, and methotrexate) within 4 weeks prior to first dose or immunosuppressants (eg, cyclosporine, tacrolimus) within 8 weeks prior to first dose.\n2. Any medicinal product, herbal medication, or natural health product which might interfere with cytochrome P450 genotype 3A4 (CYP3A4) within 2 weeks prior to enrollment, except for any CYP3A4 modulator used to treat a C. difficile or an intestinal pathogen infection at screening.\n3. Has received any of the following medical therapies for UC:\n\n 1. IV antibiotics within 8 weeks prior to enrollment.\n 2. Any rectal therapy for treatment of UC within 2 weeks prior to screening endoscopy.\n 3. Chronic NSAID use defined as daily use for \\>2 consecutive weeks (Note: occasional use \\[\\<2 consecutive weeks\\] of NSAIDs and acetaminophen \\[\\<100 mg daily\\] for headache, arthritis, myalgias, or menstrual cramps and chronic low dose aspirin use \\[81-162.5 mg daily\\] for cardiovascular prophylaxis are permitted).\n4. Has received a live vaccine within 4 weeks prior to first dose.\n\nGeneral Exclusion Criteria:\n\n1. Has any of the following cardiovascular or thrombotic conditions:\n\n 1. Recent (within past 6 months) cerebrovascular accident, myocardial infarction, or coronary stenting.\n 2. Recent (within past 6 months) moderate to severe congestive heart failure (New York Heart Association class III or IV).\n 3. Prior history of thrombotic events, including deep vein thrombosis and pulmonary embolism.\n 4. Known inherited conditions that predispose to hypercoagulability.\n2. History of lymphoproliferative disease, including lymphoma, or signs and symptoms suggestive of possible lymphoproliferative disease, such as lymphadenopathy and/or splenomegaly.\n3. A surgical procedure requiring general anesthesia within 3 months prior to screening or is planning to undergo major surgery during the study period.\n4. 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