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RECRUITING
NCT07519525
PHASE1

A Study of [14C]-LY4064809 in Healthy Participants

Sponsor: Eli Lilly and Company

View on ClinicalTrials.gov

Summary

The purpose of this study is to determine in healthy participants the percentage of LY4064809 that enters bloodstream after oral administration. Blood tests will be performed to investigate how the body processes the study drug. For each participant, the study will last about 21 days, not including screening. Participants will remain in the clinical research center for 14 days.

Official title: A Phase 1, Open-label Study of the Absolute Bioavailability of [14C]-LY4064809 in Healthy Adult Participants

Key Details

Gender

All

Age Range

18 Years - 55 Years

Study Type

INTERVENTIONAL

Enrollment

8

Start Date

2026-03-27

Completion Date

2026-05

Last Updated

2026-04-09

Healthy Volunteers

Yes

Conditions

Interventions

DRUG

LY4064809

Administered orally

DRUG

[14C]-LY4064809

Administered by IV infusion

Locations (1)

Fortrea Clinical Research Unit Inc. - Madison

Madison, Wisconsin, United States