Actively Recruiting
A Study of LY4167586 in Participants With Obesity or Overweight Who Are Otherwise Healthy
Led by Eli Lilly and Company · Updated on 2026-03-09
84
Participants Needed
2
Research Sites
54 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this study is to look at how safe and well-tolerated LY4167586 is in participants with obesity or overweight who are otherwise healthy. Blood tests will be performed to check how much LY4167586 gets into the bloodstream and how long it takes the body to eliminate it following a single administration. Participation in the study will last approximately 7 months.
CONDITIONS
Official Title
A Study of LY4167586 in Participants With Obesity or Overweight Who Are Otherwise Healthy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participant must be 21 for Singapore site
- Have a body mass index (BMI) between 27.0 kilogram per square meter (kg/m²) and 35.0 kg/m², inclusive
- Have had a self-reported stable weight for 3 months prior to screening (less than approximately 5 percent [%] body weight change)
You will not qualify if you...
- Have a history or presence of cardiovascular, respiratory, hepatic, renal, gastrointestinal (GI), endocrine, hematological, or neurological disorders capable of significantly altering the absorption, metabolism, or elimination of drugs, or of constituting a risk when taking the study drug, or of interfering with the interpretation of data.
- Is an individual of childbearing potential (IOCBP)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Fortrea Clinical Research Unit
Madison, Wisconsin, United States, 53704
Actively Recruiting
2
Lilly Centre for Clinical Pharmacology
Singapore, Singapore, 138623
Actively Recruiting
Research Team
T
Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or
CONTACT
P
Physicians interested in becoming principal investigators please contact
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
BASIC_SCIENCE
Number of Arms
3
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