drugset / Trial / NCT06709820

A Study of LY4060874 in Healthy Participants

NCT06709820 ↗

Phase 1 Completed 121 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindBasic science

Summary

The purpose of this study is to evaluate safety and tolerability of LY4060874 in healthy participants. Study participation may last up to 22 weeks and up to approximately 18 study visits.

Timeline

Start
2024-12-02
Primary completion
2026-02-20
Completion
2026-02-20

Drugs

EvaluationDrugModalityDoseRoute
Subject LY4060874 Unknown — Subcutaneous

Indications

No indication recorded.