A Study to Assess the Efficacy and Safety of Induction and Maintenance Therapy With Afimkibart (RO7790121) in Participants With Moderately to Severely Active Crohn's Disease
Purpose
This Phase III, multicenter, double-blind, placebo-controlled treat-through study will evaluate the efficacy and safety of induction and maintenance therapy with Afimkibart (also known as RO7790121) in participants with moderately to severely active Crohn's disease (CD).
Condition
- Moderately to Severely Active Crohns Disease
Eligibility
- Eligible Ages
- Between 16 Years and 80 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Confirmed diagnosis of CD - Moderately to severely active CD - Bodyweight >= 40 kilogram (kg) - Demonstrated inadequate response, loss of response and/or intolerance to at least one protocol-specified conventional or advanced CD therapy - Males and females of childbearing potential must meet protocol criteria for contraception requirements
Exclusion Criteria
- Current diagnosis of ulcerative colitis (UC) or indeterminate colitis, ischemic colitis, infectious colitis, radiation colitis, microscopic colitis - Participant with a history of >= 3 bowel resections (> 2 missing segments of the 5 following segments: terminal ilelium, right colon, transverse colon, sigmoid and left colon, and rectum) - Diagnosis of short gut or short bowel syndrome - Presence of an ileostomy, colostomy or ileoanal pouch - Participants with symptomatic bowel strictures, fulminant colitis, or toxic megacolon - Presence of abdominal or perianal abscess - Presence of rectovaginal, enterovaginal, high output enterocutaneous fistula, enterovesical fistulas or perianal fistulas with >3 openings - Current diagnosis or suspicion of primary sclerosing cholangitis - Pregnancy or breastfeeding, or intention of becoming pregnant during the study - Any past or current evidence of cancer of gastrointestinal tract, definite low-grade or high-grade colonic dysplasia - History of non-gastrointestinal cancer, with the exception of adequately treated non-metastatic basal cell or squamous cell skin cancer or in situ cervical cancer - Evidence of infection with Clostridioides difficile (C. difficile; formerly known as Clostridium difficile), cytomegalovirus (CMV), human immunodeficiency virus (HIV), Hepatitis B (HBV), Hepatitis C (HCV) during screening - Has evidence of active tuberculosis (TB), latent TB not successfully treated (per local guidance) or inadequately treated TB - Has received protocol-specified prohibited medicines, including known exposure to any type of anti-TL1A therapy
Study Design
- Phase
- Phase 3
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Primary Purpose
- Treatment
- Masking
- Double (Participant, Investigator)
Arm Groups
Arm | Description | Assigned Intervention |
---|---|---|
Experimental Arm 1: Afimkibart |
Participants will receive afimkibart intravenously (IV) followed by afimkibart subcutaneous (SC) injection. |
|
Experimental Arm 2: Afimkibart |
Participants will receive afimkibart IV followed by afimkibart SC injection. |
|
Placebo Comparator Arm 3: Placebo |
Participants will receive placebo IV followed by placebo SC. |
|
Recruiting Locations
Dothan 4059102, Alabama 4829764 36305
Sun City 5316201, Arizona 5551752 85351
Garden Grove 5351515, California 5332921 92845-2006
Inglewood 5359488, California 5332921 90301
Lancaster 5364940, California 5332921 93534
Lancaster 5364940, California 5332921 93534
Los Alamitos 5368304, California 5332921 90720
San Diego 5391811, California 5332921 92120
San Francisco 5391959, California 5332921 94115
Littleton 5429032, Colorado 5417618 80120
Lone Tree 5429208, Colorado 5417618 80124
Brooksville 4148986, Florida 4155751 34613
Clearwater 4151316, Florida 4155751 33756
Coral Gables 4151871, Florida 4155751 33134
Coral Gables 4151871, Florida 4155751 33134
Hialeah 4158476, Florida 4155751 33013
Hialeah 4158476, Florida 4155751 33016
Kissimmee 4160983, Florida 4155751 34741
Lakewood Rch 7255365, Florida 4155751 34211
Miami 4164138, Florida 4155751 33126
Miami 4164138, Florida 4155751 33176
Orlando 4167147, Florida 4155751 32806
Tampa 4174757, Florida 4155751 33607
Tampa 4174757, Florida 4155751 33612
Tampa 4174757, Florida 4155751 33614
Temple Terrace 4174969, Florida 4155751 33617-1666
Atlanta 4180439, Georgia 4197000 30327
Atlanta 4180439, Georgia 4197000 30342
Macon 4207400, Georgia 4197000 31201
Idaho Falls 5596475, Idaho 5596512 83404
Glenview 4893886, Illinois 4896861 60026
Gurnee 4894861, Illinois 4896861 60031
Indianapolis 4259418, Indiana 4921868 46202
New Albany 4262045, Indiana 4921868 47150
Wichita 4281730, Kansas 4273857 67226
Crestview Hills 4289040, Kentucky 6254925 41017-3409
Louisville 4299276, Kentucky 6254925 40218
Boston 4930956, Massachusetts 6254926 02115
Farmington Hills 4992523, Michigan 5001836 48334
Oxford 4440076, Mississippi 4436296 38655
Southaven 4446675, Mississippi 4436296 38671
North Las Vegas 5509403, Nevada 5509151 89030
New York 5128581, New York 5128638 10075
North Massapequa 5129134, New York 5128638 11758
Queens Village 5133271, New York 5128638 11428
Richmond Hill 5133825, New York 5128638 11418
Rochester 5134086, New York 5128638 14618
Fuquay-Varina 4467485, North Carolina 4482348 27526
Monroe 4479946, North Carolina 4482348 28112
Beavercreek 4506008, Ohio 5165418 45440
Columbus 4509177, Ohio 5165418 43202
Columbus 4509177, Ohio 5165418 43210
Westlake 5176517, Ohio 5165418 44145
Norman 4543762, Oklahoma 4544379 73071
Uniontown 4561859, Pennsylvania 6254927 15401-9069
Providence 5224151, Rhode Island 5224323 02904
Greenville 4580543, South Carolina 4597040 29607
Germantown 4624601, Tennessee 4662168 38138
Nashville 4644585, Tennessee 4662168 37211
Arlington 4671240, Texas 4736286 76012
El Paso 5520993, Texas 4736286 79902
Georgetown 4693342, Texas 4736286 78628
Harlingen 4696233, Texas 4736286 78550
Mansfield 4709013, Texas 4736286 76063
Mesquite 4710826, Texas 4736286 75149
San Antonio 4726206, Texas 4736286 78229
Southlake 4733313, Texas 4736286 76092
Tyler 4738214, Texas 4736286 75701
Chesapeake 4752186, Virginia 6254928 23320
Lansdowne Town Center 7309207, Virginia 6254928 20176
Roanoke 4782167, Virginia 6254928 24014
Williamsburg 4793846, Virginia 6254928 23188-2862
Vancouver 5814616, Washington 5815135 98664
San Juan 4568127, Puerto Rico 00909
More Details
- NCT ID
- NCT06819878
- Status
- Recruiting
- Sponsor
- Hoffmann-La Roche
Study Contact
Reference Study ID Number: GA45331 https://forpatients.roche.com/888-662-6728 (U.S. and Canada)
global-roche-genentech-trials@gene.com