A Study of Brenipatide (LY3537031) in Healthy Participants With Overweight or Obesity (NCT07476118) | Clinical Trial Compass
RecruitingPhase 1
A Study of Brenipatide (LY3537031) in Healthy Participants With Overweight or Obesity
United States150 participantsStarted 2026-03-18
Plain-language summary
The main purpose of this study is to evaluate how different dose levels of brenipatide work and how safe they are in healthy people with overweight or obesity. The study will assess the effects of different doses given as subcutaneous (under the skin) injections. Participation in this study will last about 42 weeks.
Who can participate
Age range18 Years – 65 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Are overtly healthy with no comorbidities related to body mass index (BMI), such as type 2 diabetes mellitus or unstable cardiovascular disease, as determined by medical evaluation
* Have a BMI within the range of 27.0 to 45.0 kilogram per square meter (kg/m\^2)
* Have no significant (not more than 5 percent \[%\]) self-reported weight gain or loss in the past 3 months prior to screening
Exclusion Criteria:
* Have significant history or presence of cardiovascular, respiratory, hepatic, renal, gastrointestinal (GI), endocrine, hematological, dermatological, or neurological disorders capable of significantly altering the absorption, metabolism, or elimination; constituting a risk when taking the Investigational Medical Product (IMP); or interfering with the interpretation of data
* Have a prior diagnosis of type 1 or type 2 diabetes mellitus
* Have a history of acute or chronic pancreatitis
* Have a personal or family history of medullary thyroid carcinoma or have multiple endocrine neoplasia syndrome type 2
* Have received a glucagon-like peptide-1 (GLP-1) receptor agonist, glucose-dependent insulinotropic polypeptide (GIP)/GLP-1 receptor agonist, GIP/GLP-1/glucagon receptor agonist, or amylin receptor agonist within 6 months prior to screening
* Have been treated with prescription and over-the-counter medications, or alternative remedies (including herbal/nutritional supplements), that promote weight loss within 6 months prior to screening
* Are pregn…
What they're measuring
1
Percent Change in Body Weight
Timeframe: Week 1, Week 29
Trial details
NCT IDNCT07476118
SponsorEli Lilly and Company
Sponsor typeINDUSTRY
Study typeINTERVENTIONAL
Primary completion2027-02
Contact for this trial
Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559)