Clinical Trial

A Study of LY4515100 in Healthy Participants

Recruiting Phase 1
View on ClinicalTrials.gov →
Summary
The main purpose of this study is to assess the safety and tolerability of LY4515100 when given orally to healthy participants. LY4515100 will be given by itself or with other medicines. Blood tests will be performed to investigate how the body processes the study drug and how the study drug affects the body. The study will have 3 parts and will last about 50 days. For each participant in Part A, the study will include a stay in the Clinical Research Unit (CRU) lasting about 6 days. For each participant in Part B, the study will include a stay in the CRU lasting about 15 days. For each participant in Part C, the study will include up to 2 stays in the CRU each lasting between 7-28 days.
Protocol Amendment History 5 changes
critical Primary endpoint(s) modified 2026-07-30
notable Enrollment increased: 40 -> 123 participants 2026-07-30
minor Trial arms changed: 4 -> 7 2026-07-30
notable Primary completion pushed: 2026-07 -> 2027-03 2026-07-30
minor Completion pushed: 2026-07 -> 2027-03 2026-07-30
Trial Details
NCT Number NCT07339722
Lead Sponsor Eli Lilly and Company
Conditions Healthy
Enrollment 123 participants
Start Date 2026-01-15
Primary Completion 2027-03 (estimated)
Study Completion 2027-03 (estimated)
Updated on ClinicalTrials.gov 2026-07-29