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A Study of LY4005130 in Healthy Participants
Sponsor: Eli Lilly and Company
Summary
The purpose of this study is to evaluate how well LY4005130 is tolerated and what side effects may occur in healthy participants. The study drug will be administered either subcutaneously (SC) (under the skin) or intravenously (IV) (into a vein in the arm). Blood tests will be performed to check how much LY4005130 gets into the bloodstream and how long it takes the body to eliminate it. Part A for the single-ascending doses (SAD) of the study will last about 12 weeks with 9 visits. Part B for the multiple-ascending doses (MAD) of the study will either last about 16 weeks with 13 visits or 26 weeks with 14 visits not including screening.
Official title: A Phase 1, Randomized, Placebo-controlled, Investigator and Participant Blinded, Single-ascending Dose and Multiple-ascending Dose Study to Evaluate Safety, Tolerability, and Pharmacokinetics of LY4005130 in Healthy Participants.
Key Details
Gender
All
Age Range
18 Years - 65 Years
Study Type
INTERVENTIONAL
Enrollment
118
Start Date
2024-11-08
Completion Date
2026-04
Last Updated
2025-11-10
Healthy Volunteers
Yes
Conditions
Interventions
LY4005130
Administered IV
LY4005130
Administered SC
Placebo
Administered IV
Placebo
Administered SC
Locations (1)
Fortrea Clinical Research Unit
Dallas, Texas, United States