Crohn's Disease Clinical Trials

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A Phase 2 Platform Basket Study Evaluating Advanced Therapies in Subjects With Moderately to Severely Active Crohn's Disease or Ulcerative Colitis

Status: Recruiting
Location: See all (66) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

⁃ 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

Locations
United States
Alabama
Digestive Health Specialists /ID# 280827
RECRUITING
Dothan
Arizona
Elite Clinical Studies /ID# 280477
RECRUITING
Phoenix
Gi Alliance - Arizona Digestive Health - Sun City /ID# 284084
RECRUITING
Sun City
California
Clinnova Research /ID# 280509
RECRUITING
Anaheim
Southern California Res. Ctr /ID# 280476
RECRUITING
Coronado
Gastro Care Institute /ID# 281071
RECRUITING
Lancaster
United Medical Doctors - Los Alamitos /ID# 281125
RECRUITING
Los Alamitos
Inland Empire Liver Foundation - Rialto /ID# 280775
RECRUITING
Rialto
Colorado
Peak Gastroenterology Associates - Colorado Springs - North Cascade Avenue /ID# 280507
RECRUITING
Colorado Springs
Florida
Synergy Healthcare - Bradenton /ID# 284157
RECRUITING
Bradenton
Clinical Research of Osceola /ID# 280593
RECRUITING
Kissimmee
Florida Center For Gastroenterology - Largo /ID# 281059
RECRUITING
Largo
Research Associates of South Florida /ID# 280929
RECRUITING
Miami
Advanced Research Institute, Inc /ID# 281062
RECRUITING
New Port Richey
Digestive And Liver Center Of Florida - Orlando /ID# 280924
RECRUITING
Orlando
Gcp Clinical Research /ID# 280469
RECRUITING
Tampa
Georgia
Gastroenterology Associates of Central Georgia /ID# 280464
RECRUITING
Macon
Gastroenterology Consultants - Roswell /ID# 281235
RECRUITING
Roswell
Idaho
Treasure Valley Medical Research /ID# 281778
RECRUITING
Boise
Illinois
Midwest Digestive Health & Nutrition /ID# 285250
RECRUITING
Des Plaines
Gi Alliance - Glenview /ID# 283932
RECRUITING
Glenview
Illinois Gastroenterology Group /ID# 283933
RECRUITING
Gurnee
Southwest Gastroenterology - Oak Lawn /ID# 280841
RECRUITING
Oak Lawn
Indiana
Gastroenterology Health Partners /ID# 284145
RECRUITING
New Albany
Kentucky
Gastroenterology Health Partners /ID# 284144
RECRUITING
Louisville
Louisiana
Gastro Group and Endocenter: Mandeville, la /ID# 284186
RECRUITING
Mandeville
Metropolitan Gastroenterology Associates - Metairie /ID# 283922
RECRUITING
Metairie
Willis-Knighton Medical Center /ID# 280572
RECRUITING
Shreveport
Massachusetts
Lucida Clinical Trials /ID# 282000
RECRUITING
New Bedford
Michigan
West Michigan Clinical Research Center /ID# 280480
RECRUITING
Wyoming
Missouri
Specialists In Gastroenterology /ID# 283939
RECRUITING
St Louis
Mississippi
Gi Associates - Gia And Endoscopy Center - Flowood /ID# 283967
RECRUITING
Flowood
Gastroenterology Associates Of North Mississippi /ID# 285243
RECRUITING
Oxford
North Carolina
Digestive Health Partners /ID# 280490
RECRUITING
Asheville
Nevada
Vector Clinical Trials /ID# 280843
RECRUITING
Las Vegas
New York
New York Gastroenterology Associates - Upper East Side /ID# 281767
RECRUITING
New York
Ohio
Dayton Gastroenterology - Beavercreek /ID# 284065
RECRUITING
Beavercreek
Gastro Intestinal Research Institute of Northern Ohio /ID# 283860
RECRUITING
Westlake
Rhode Island
University Gastroenterology - Providence - Staniford Street /ID# 280919
RECRUITING
Providence
South Carolina
Gastroenterology Associates - Patewood /ID# 283870
RECRUITING
Greenville
Tennessee
Gastrointestinal Associates - Knoxville - Dowell Springs Boulevard /ID# 283861
RECRUITING
Knoxville
Gastro One - Memphis /ID# 283948
RECRUITING
Memphis
Texas
Novel Research - Bellaire /ID# 280925
RECRUITING
Bellaire
Gi Alliance - Texas Digestive Disease Consultants - Fort Worth /ID# 283977
RECRUITING
Fort Worth
GI Alliance -Garland /ID# 284253
RECRUITING
Garland
Amel Med /ID# 283864
RECRUITING
Georgetown
Integrity Advanced Therapeutics /ID# 283871
RECRUITING
Houston
Caprock Gastro Research - Lubbock /ID# 283921
RECRUITING
Lubbock
GI Alliance - Lubbock /ID# 283920
RECRUITING
Lubbock
GI Alliance - Mansfield /ID# 283924
RECRUITING
Mansfield
Southern Star Research Institute /ID# 280822
RECRUITING
San Antonio
Center for Digestive Disease /ID# 280870
RECRUITING
Shenandoah
Texas Digestive Disease Consultants - Southlake /ID# 283931
RECRUITING
Southlake
Tyler Research Institute /ID# 284247
RECRUITING
Tyler
Texas Digestive Disease Consultants /ID# 284245
RECRUITING
Webster
Virginia
Emeritas Research Group /ID# 284388
RECRUITING
Lansdowne Town Center
GI Alliance - Richmond /ID# 284244
RECRUITING
Richmond
Washington
Washington Gastroenterology - Bellevue /ID# 283966
RECRUITING
Bellevue
Washington Gastroenterology - Tacoma /ID# 284143
RECRUITING
Tacoma
The Vancouver Clinic /ID# 280497
RECRUITING
Vancouver
Wisconsin
Wisconsin Center for Advanced Research /ID# 284250
RECRUITING
Milwaukee
Other Locations
Canada
Diex Recherche Quebec Inc. /ID# 282307
RECRUITING
Québec
Israel
Assuta Ashdod Medical Center /ID# 280535
RECRUITING
Ashdod
Japan
Kure Kyosai Hospital /ID# 282006
RECRUITING
Kure
Taiwan
Kaohsiung Medical University Chung-Ho Memorial Hospital /ID# 280640
RECRUITING
Kaohsiung City
China Medical University Hospital /ID# 280630
RECRUITING
Taichung
Contact Information
Primary
ABBVIE CALL CENTER
abbvieclinicaltrials@abbvie.com
844-663-3742
Time Frame
Start Date: 2026-07-31
Estimated Completion Date: 2031-10
Participants
Target number of participants: 2000
Treatments
Experimental: Substudy 1: UC Arm 1 Risankizumab monotherapy
Ulcerative Colitis (UC) participants will receive Risankizumab Dose A as induction treatment followed by Risankizumab Dose C as maintenance treatment.
Experimental: Substudy 1: CD Arm 1 Risankizumab monotherapy
Crohn's Disease (CD) participants will receive Risankizumab Dose B as induction treatment followed by Risankizumab Dose D as maintenance treatment.
Experimental: Substudy 1: UC Arm 2 Trosunilimab monotherapy
Ulcerative Colitis (UC) participants will receive Trosunilimab Dose A as induction treatment followed by Trosunilimab Dose C as maintenance treatment.
Experimental: Substudy 1: CD Arm 2 Trosunilimab monotherapy
Crohn's Disease (CD) participants will receive Trosunilimab Dose B as induction treatment followed by Trosunilimab Dose D as maintenance treatment.
Experimental: Substudy 1: UC Arm 3 Trosunilimab monotherapy
Ulcerative Colitis (UC) participants will receive Trosunilimab Dose E as induction treatment followed by Trosunilimab Dose G as maintenance treatment.
Experimental: Substudy 1: CD Arm 3 Trosunilimab monotherapy
Crohn's Disease (CD) participants will receive Trosunilimab Dose F as induction treatment followed by Trosunilimab Dose H as maintenance treatment.
Experimental: Substudy 1: UC Arm 4 ABBV-466 (Risankizumab/Trosunilimab)
Ulcerative Colitis (UC) participants will receive a combination induction treatment of ABBV-466 (Risankizumab/Trosunilimab) combo Dose A followed by a combination maintenance (Risankizumab/Trosunilimab) combo Dose C
Experimental: Substudy 1: CD Arm 4 ABBV-466 (Risankizumab/Trosunilimab)
Crohn's Disease (CD) participants will receive a combination induction treatment of ABBV-466 (Risankizumab/Trosunilimab) combo Dose B followed by a combination maintenance (Risankizumab/Trosunilimab) combo Dose D
Experimental: Substudy 1: UC Arm 5 ABBV-466 (Risankizumab/Trosunilimab)
Ulcerative Colitis (UC) participants will receive a combination induction treatment of ABBV-466 (Risankizumab/Trosunilimab) combo Dose E followed by a combination maintenance (Risankizumab/Trosunilimab) combo Dose G
Experimental: Substudy 1: CD Arm 5 ABBV-466 (Risankizumab/Trosunilimab)
Crohn's Disease (CD) participants will receive a combination induction treatment of ABBV-466 (Risankizumab/Trosunilimab) combo Dose F followed by a combination maintenance (Risankizumab/Trosunilimab) combo Dose H
Experimental: Substudy 2: UC Arm 1 Risankizumab monotherapy
Ulcerative Colitis (UC) participants will receive Risankizumab Dose A as induction treatment followed by Risankizumab Dose C as maintenance treatment.
Experimental: Substudy 2: CD Arm 1 Risankizumab monotherapy
Crohn's Disease (CD) participants will receive Risankizumab Dose B as induction treatment followed by Risankizumab Dose D as maintenance treatment.
Experimental: Substudy 2: UC Arm 2 ABBV-701 monotherapy
Ulcerative Colitis (UC) participants will receive ABBV-701 Dose A as induction treatment and Dose C maintenance treatment.
Experimental: Substudy 2: CD Arm 2 ABBV-701 monotherapy
Crohn's Disease (CD) participants will receive ABBV-701 Dose B as induction treatment and Dose D maintenance treatment.
Experimental: Substudy 2: UC Arm 3 ABBV-701 monotherapy
Ulcerative Colitis (UC) participants will receive ABBV-701 Dose E as induction treatment and Dose G maintenance treatment.
Experimental: Substudy 2: CD Arm 3 ABBV-701 monotherapy
Crohn's Disease (CD) participants will receive ABBV-701 Dose F as induction treatment and Dose H maintenance treatment.
Experimental: Substudy 2: UC Arm 4 ABBV-7066 (Risankizumab/ABBV-701)
Ulcerative Colitis (UC) participants will receive induction treatment of ABBV-7066 (Risankizumab/ABBV-701) combination Dose A followed by maintenance treatment of ABBV-7066 (Risankizumab/ABBV-701) combination Dose C.
Experimental: Substudy 2: CD Arm 4 ABBV-7066 (Risankizumab/ABBV-701)
Crohn's Disease (CD) participants will receive induction treatment of ABBV-7066 (Risankizumab/ABBV-701) combination Dose B followed by maintenance treatment of ABBV-7066 (Risankizumab/ABBV-701) combination Dose D.
Experimental: Substudy 2: UC Arm 5 ABBV-7066 (Risankizumab/ABBV-701)
Ulcerative Colitis (UC) participants will receive induction treatment of ABBV-7066 (Risankizumab/ABBV-701) combination Dose E followed by maintenance treatment of ABBV-7066 (Risankizumab/ABBV-701) combination Dose G.
Experimental: Substudy 2: CD Arm 5 ABBV-7066 (Risankizumab/ABBV-701)
Crohn's Disease (CD) participants will receive induction treatment of ABBV-7066 (Risankizumab/ABBV-701) combination Dose F followed by maintenance treatment of ABBV-7066 (Risankizumab/ABBV-701) combination Dose H.
Experimental: Substudy 2: UC Arm 6 ABBV-7066 (Risankizumab/ABBV-701)
Ulcerative Colitis (UC) participants will receive induction treatment of ABBV-7066 (Risankizumab/ABBV-701) combination Dose I followed by maintenance treatment of ABBV-7066 (Risankizumab/ABBV-701) combination Dose J
Experimental: Substudy 2: CD Arm 6 ABBV-7066 (Risankizumab/ABBV-701)
Crohn's Disease (CD) participants will receive induction treatment of ABBV-7066 (Risankizumab/ ABBV-701) combination Dose K followed by maintenance treatment of ABBV-7066 (Risankizumab/ ABBV-701) combination Dose L
Sponsors
Leads: AbbVie

This content was sourced from clinicaltrials.gov

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