A Clinical Study of Tulisokibart (MK-7240) to Treat Radiographic Axial Spondyloarthritis (MK-7240-013)
Merck Sharp & Dohme LLC · NCT07133633
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–80 · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 2
- Target enrollment
- 315
- US sites recruiting
- 36
- Study start
- September 26, 2025
- Record last updated
- October 23, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
Researchers are looking for new ways to treat radiographic axial spondyloarthritis (r-axSpA). R-axSpA is a type of arthritis that causes pain, stiffness, and inflammation (swelling) in the spine and joints in the pelvis (hip bone). Radiographic means the damage it causes can be seen on X-rays.
This study will help find out if a study medicine called tulisokibart can treat symptoms of r-axSpA. Researchers will look at different doses of tulisokibart.
Researchers want to know if at least one of the study doses of tulisokibart works better than a placebo to improve r-axSpA symptoms. A placebo looks like the study medicine but has no study medicine in it. Using a placebo helps researchers better understand the effects of the study medicine.
Being studied: Tulisokibart; Placebo
Conditions: Radiographic Axial Spondyloarthritis
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
The main inclusion criteria include but are not limited to the following:
- Has a clinical diagnosis of axial spondyloarthritis (axSpA) and meets the Assessment of SpondyloArthritis international Society (ASAS) classification criteria for axSpA including ≥3 months of back pain with age at symptom onset \<45 years
- Meets the radiographic criterion of the modified New York criteria for ankylosing spondylitis (AS) as determined by central reading at Screening
- Has active disease at Screening and Randomization
- Has a history of inadequate response (IR)/intolerance to nonsteroidal anti-inflammatory drugs (NSAIDs) and is biologic disease-modifying antirheumatic drug (bDMARD)-naive, or has a history of IR/intolerance to up to a maximum of 2 bDMARD classes
Exclusion Criteria
The main exclusion criteria include but are not limited to the following:
- Has any arthritis with onset before age 17 years or current diagnosis of inflammatory joint disease other than radiographic axial spondyloarthritis (r-axSpA) (such as, but not limited to, rheumatoid arthritis, systemic lupus erythematosus, psoriatic arthritis (PsA), systemic sclerosis, myositis, etc.), or any other conditions that may, in the judgment of the investigator, interfere with the assessment of r-axSpA
- Has a history of cancer (except fully treated non-melanoma skin cancers or cervical carcinoma in situ after complete surgical removal) within the last 5 years
- Has any active infection
- Has known allergies, hypersensitivity, or intolerance to tulisokibart or its excipients
Recruiting US locations
AARA Clinical Research - Arizona Arthritis & Rheumatology Associates - Chandler ( Site 0036)
Chandler, AZ 85225
Site contact: Study Coordinator · 480-443-8400
AARA Clinical Research - Arizona Arthritis & Rheumatology Associates - Flagstaff ( Site 0021)
Flagstaff, AZ 86001
Site contact: Study Coordinator · 480-443-8400
Arizona Arthritis & Rheumatology Associates, P.C. - Gilbert ( Site 0022)
Gilbert, AZ 85297
Site contact: Study Coordinator · 480-443-8400
AARA Arizona Arthritis & Rheumatology Associates, P.C. - Glendale ( Site 0056)
Glendale, AZ 85306
Site contact: Study Coordinator · 480-443-8400
Arizona Arthritis & Rheumatology Associates, P.C. - Tucson ( Site 0025)
Tucson, AZ 85704-1140
Site contact: Study Coordinator · 480-443-8400
Providence Medical Foundation ( Site 0049)
Fullerton, CA 92835
Site contact: Study Coordinator · 714-626-8610
Newport Huntington Medical Group ( Site 0005)
Huntington Beach, CA 92648
Site contact: Study Coordinator · 714-378-2440
Cohen Medical Centers ( Site 0034)
Thousand Oaks, CA 91360-3967
Site contact: Study Coordinator · 713-487-8680
Inland Rheumatology Clinical Trials, Inc. ( Site 0002)
Upland, CA 91786
Site contact: Study Coordinator · 909-296-8700
Denver Arthritis Clinic ( Site 0064)
Denver, CO 80230
Site contact: Study Coordinator · 303-394-2828
Arthritis and Rheumatic Disease Specialties ( Site 0016)
Aventura, FL 33180
Site contact: Study Coordinator · 305-932-4295
Bay Area Arthritis and Osteoporosis ( Site 0041)
Brandon, FL 33511
Site contact: Study Coordinator · 813-651-4441 Ext 243
GNP Research - Hollywood ( Site 0020)
Cooper City, FL 33024
Site contact: Study Coordinator · 754-248-3589
Innovation Medical Research Center ( Site 0012)
Palmetto Bay, FL 33157
Site contact: Study Coordinator · 305-300-2695
Chicago Arthritis & Regenerative Medicine ( Site 0042)
Chicago, IL 60661
Site contact: Study Coordinator · 480-443-8400
Willow Rheumatology and Wellness, PLLC ( Site 0035)
Willowbrook, IL 60527
Site contact: Study Coordinator · 630-537-1313
John Hopkins University ( Site 0052)
Baltimore, MD 21224
Site contact: Study Coordinator · 410-550-0579
Arthritis and Rheumatism Associates - Rockville ( Site 0019)
Rockville, MD 20850
Site contact: Study Coordinator · 301-942-7600
Kansas City Physician Partners ( Site 0027)
Kansas City, MO 64111
Site contact: Study Coordinator · 816-384-2827
Velocity Clinical Research - West County Rheumatology, St. Louis ( Site 0038)
St Louis, MO 63131
Site contact: Study Coordinator · 314-987-2980
Logan Health Rheumatology ( Site 0015)
Kalispell, MT 59901
Site contact: Study Coordinator · 406-752-2010
Physician Research Collaboration, LLC ( Site 0057)
Lincoln, NE 68516-5497
Site contact: Study Coordinator · 402-420-3442
Inspire Santa Fe Medical Group ( Site 0011)
Santa Fe, NM 87505
Site contact: Study Coordinator · 505-490-5984
Oregon Health & Science University ( Site 0059)
Portland, OR 97239
Site contact: Study Coordinator · 503-494-8637
Altoona Center for Clinical Research ( Site 0004)
Duncansville, PA 16635
Site contact: Study Coordinator · 814-693-0300
Perelman Center for Advanced Medicine ( Site 0060)
Philadelphia, PA 19104
Site contact: Study Coordinator · 215-662-2454
AARA Clinical Research - Murfreesboro Medical Clinic ( Site 0029)
Murfreesboro, TN 37128
Site contact: Study Coordinator · 615-236-2504
Rheumatology Associates ( Site 0055)
Arlington, TX 76012
Site contact: Study Coordinator · 214-540-0700
Arthritis Care of Texas ( Site 0048)
Corpus Christi, TX 78415
Site contact: Study Coordinator · 361-400-7700
Lone Star Arthritis & Rheumatology Associates, P.C. ( Site 0028)
Fort Worth, TX 76109
Site contact: Study Coordinator · 301-942-7600
Provecta Research Network LLC ( Site 0054)
Houston, TX 77027
Site contact: Study Coordinator · 346-735-8990
The University of Texas Health Science Center at Houston ( Site 0065)
Houston, TX 77030
Site contact: Study Coordinator · 713-500-6597
AARA Clinical Research - Lone Star Arthritis and Rheumatology Associates - Irving ( Site 0032)
Irving, TX 75039
Site contact: Study Coordinator · 301-942-7600
Epic Medical Research ( Site 0061)
Red Oak, TX 75154
Site contact: Study Coordinator · 972-777-6956
Advanced Rheumatology of Houston ( Site 0001)
The Woodlands, TX 77382
Site contact: Study Coordinator · 936-681-4882
DM Clinical Research - TRA ( Site 0010)
Tomball, TX 77375
Site contact: Study Coordinator · 346-550-9559
Study contacts (from the official record)
- Toll Free Number · 1-888-577-8839 · Trialsites@msd.com
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