RecruitingPhase 1NCT07566338

A Study of LY4302814 in Healthy Participants

A Phase 1, Randomized, Placebo-Controlled, Investigator and Participant Blinded, Single Ascending Dose and Multiple Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LY4302814 in Healthy Participants


Sponsor

Eli Lilly and Company

Enrollment

150 participants

Start Date

May 6, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The main purpose of this study is to assess how well LY4302814 is tolerated and what side effects may occur in healthy participants. Blood tests will be performed to investigate how the body processes the study drug and how the study drug affects the body. For each participant, the study will last about 6 months and will include at least one overnight stay in the clinical research unit (CRU) lasting up to approximately 9 days.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called LY4302814, a drug called LY4302814, and others for people with healthy. The study is currently recruiting participants at 2 locations. People eligible for this study include aged 18 Years to 65 Years.

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

DRUGLY4302814

Administered SC

DRUGLY4302814

Administered IV

DRUGPlacebo

Administered SC

DRUGPlacebo

Administered IV


Locations(2)

Fortrea Clinical Research Unit

Daytona Beach, Florida, United States

Lilly Centre for Clinical Pharmacology

Singapore, Singapore

View Full Details on ClinicalTrials.gov

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NCT07566338


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