RecruitingPhase 1NCT07232732

A Study of LY3549492 in Healthy Participants and Participants With Overweight or Obesity

A Phase-1, Parallel-Design, Open-Label, Randomized, Multiple-Dose Escalation Study to Investigate the Safety, Tolerability, and Pharmacokinetics of LY3549492 in Healthy Participants With Overweight or Obesity


Sponsor

Eli Lilly and Company

Enrollment

120 participants

Start Date

Oct 27, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to see how safe and well-tolerated the drug LY3549492 is and how it behaves in the body, when given in multiple doses to healthy people who are overweight or have obesity. Participation in the study will last approximately 8 weeks.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This Phase 1 study evaluates the safety and how the body handles a new investigational drug called LY3549492, which is being explored as a potential treatment for overweight or obesity. Multiple doses are given to assess how the drug is absorbed, distributed, and cleared by the body, and to identify any side effects. Adults with a BMI between 25 and 45 kg/m², no diabetes (HbA1c below 6.5%), and no recent serious cardiovascular events or prior GLP-1 medication use within 3 months may be eligible. Participation lasts approximately 8 weeks and involves receiving daily doses of the study drug and attending clinic visits for blood tests and safety monitoring. This summary was generated by AI to help patients understand the study in plain language.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGLY3549492

Administered orally


Locations(3)

Fortrea Clinical Research Unit

Daytona Beach, Florida, United States

Fortrea Clinical Research Unit

Dallas, Texas, United States

Fortrea Clinical Research Unit

Madison, Wisconsin, United States

View Full Details on ClinicalTrials.gov

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NCT07232732


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