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Active Not RecruitingNCT07339735

A Study of LY4064809 in Healthy Adult Participants

A Phase 1, Open-Label Study to Assess the Relative Bioavailability of Two LY4064809 Formulations in Healthy Adult Participants

Status
Active Not Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
24 (estimated)
Sponsor
Eli Lilly and Company · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to find out how much LY4064809 gets into the blood stream and how long it takes the body to get rid of it when it is given as two formulations. For each participant, the study will last about nine weeks. Participants will remain in the clinical research center for about one month.

Conditions

Interventions

TypeNameDescription
DRUGLY4064809 Test FormulationAdministered orally
DRUGLY4064809 Reference FormulationAdministered orally

Timeline

Start date
2026-01-12
Primary completion
2026-03-01
Completion
2026-03-01
First posted
2026-01-14
Last updated
2026-03-02

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT07339735. Inclusion in this directory is not an endorsement.