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ACTIVE NOT RECRUITING
NCT06690996
PHASE1

A Study of LY4005130 in Healthy Participants

Sponsor: Eli Lilly and Company

View on ClinicalTrials.gov

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

DRUG

LY4005130

Administered IV

DRUG

LY4005130

Administered SC

DRUG

Placebo

Administered IV

DRUG

Placebo

Administered SC

Locations (1)

Fortrea Clinical Research Unit

Dallas, Texas, United States