Efficacy and Safety of Eloralintide (LY3841136) in Participants With Osteoarthritis Knee Pain and Obesity or Overweight
Eli Lilly and Company · NCT07353931
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+ · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 3
- Target enrollment
- 900
- US sites recruiting
- 38
- Study start
- February 9, 2026
- Record last updated
- October 8, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The YDAN master protocol will support two independent studies, J3R-MC-YOA1 and J3R-MC-YOA2. Each study will investigate how well and safely Eloralintide (LY3841136) works in adults with obesity or overweight who have osteoarthritis (OA) of the knee with pain. Participation in the study will last about 75 weeks, including screening.
Being studied: Eloralintide; Placebo
Conditions: Osteoarthritis; Overweight or Obesity
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Have a body mass index (BMI) of 27 kilograms per square meter (kg/m²) or higher at screening
- Have a stable body weight (less than 5% body weight change) for 90 days prior to screening
- Have tried at least once to lose weight through diet but were unsuccessful
- Have osteoarthritis of the knee and at least one of the following conditions:
- Be over 50 years old
- Have morning knee stiffness that lasts about 30 minutes
- Have a crackling or grinding sound or feeling in the knee
Exclusion Criteria
- Have a prior or planned surgical treatment for obesity (liposuction, cryolipolysis, or abdominoplasty allowed if performed greater than 1 year before screening)
- Have a prior or planned endoscopic procedure and/or device-based therapy for obesity (prior device-based therapy acceptable if device removal was more than 6 months prior to screening)
- Have type 1 diabetes, type 2 diabetes, or any other type of diabetes
- Have an active knee infection
- Have had within 90 days prior to screening:
- heart attack
- stroke
- coronary artery revascularization
- unstable angina, or
- hospitalization due to congestive heart failure
- Have a history or diagnosis of New York Heart Association Functional Classification Class IV congestive heart failure
- Have taken medications or alternative remedies intended for weight loss within 90 days of screening
Recruiting US locations
AMR Clinical
Mobile, AL 36608
Site contact: 251-414-1984
Care Access - 801 South Power Road, Mesa
Mesa, AZ 85206
Site contact: 877-791-0656
Elite Pain and Spine Institute - South Crimson Road
Mesa, AZ 85209
Site contact: Zeeshan Malik
Elite Clinical Studies, LLC
Phoenix, AZ 85018
Site contact: 602-788-3437
Tucson Orthopaedic Institute - North Wyatt Drive
Tucson, AZ 85712
Site contact: 520-404-0276
Ark Clinical Research - Fountain Valley
Fountain Valley, CA 92708
Site contact: 714-988-2021
Wolverine Clinical Trials
Santa Ana, CA 92706
Site contact: 714-617-2426
Encompass Clinical Research
Spring Valley, CA 91978
Site contact: 619-660-9068
Diablo Clinical Research, Inc.
Walnut Creek, CA 94598
Site contact: 925-930-7267
Skylight Health Research - Colorado Springs
Colorado Springs, CO 80917
Site contact: Renee Flick
Westside Center for Clinical Research
Jacksonville, FL 32205
Site contact: 904-693-1490
Care Access - St. Petersburg
St. Petersburg, FL 33710
Site contact: 877-791-0656
Conquest Research
Winter Park, FL 32789
Site contact: 407-916-0060
Orita Clinical Research
Decatur, GA 30034
Site contact: Ahmad Jingo
Medical Research Partners
Ammon, ID 83406
Site contact: 208-681-9070
Great Lakes Clinical Trials - Ravenswood
Chicago, IL 60640
Site contact: 773-275-3500
Qualmedica Research, LLC
Evansville, IN 47715
Site contact: 812-205-2475
AMR Clinical
Newton, KS 67114
Site contact: 316-804-7304
Monroe Biomedical Research - Louisville
Louisville, KY 40213
Site contact: 502-515-5672
Skylight Health Research - Burlington
Burlington, MA 01803
Site contact: 781-653-4281
Care Access - Quincy
Quincy, MA 02169
Site contact: 877-791-0656
Ellipsis Research Group - Brooklyn - 7th Street
Brooklyn, NY 11215
Site contact: 347-422-0317
Rochester Clinical Research - Buffalo
Buffalo, NY 14127
Site contact: Rajiv Jain
NYC Research INC
Long Island City, NY 11106
Site contact: 516-574-9232
Rochester Clinical Research, LLC
Rochester, NY 14609
Site contact: 585-288-0890
Central States Research
Tulsa, OK 74136
Site contact: 918-645-5400
Keystone Clinical Studies
Plymouth Meeting, PA 19462
Site contact: Cameron Olezene
JCCT - Juno Bellaire Site
Bellaire, TX 77401
Site contact: 713-779-5494
Epic Medical Research - DeSoto
DeSoto, TX 75115
Site contact: 197-277-7695
Valley Institute of Research - Fort Worth
Fort Worth, TX 76164
Site contact: 817-625-7733
Care Access - Houston
Houston, TX 77054
Site contact: 877-791-0656
VIP Trials
San Antonio, TX 78230
Site contact: 210-569-2672
Endeavor Clinical Trials
San Antonio, TX 78240
Site contact: 518-428-6859
Consano Clinical Research, LLC
Shavano Park, TX 78231
Site contact: 210-545-4900
Texas Valley Clinical Research
Weslaco, TX 78596
Site contact: 956-431-8090
AMR Clinical
South Jordan, UT 84095
Site contact: Curtis Andrews
Charlottesville Medical Research
Charlottesville, VA 22911
Site contact: 434-817-2442
Paramount Clinical Research - Data Point Clinical Research
Kirkland, WA 98034
Site contact: 425-577-1107
Study contacts (from the official record)
- Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or · 317-615-4559 · LillyTrials@Lilly.com
- Physicians interested in becoming principal investigators please contact · clinical_inquiry_hub@lilly.com
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