drugset / Trial / NCT05492201

A Study of LY3873862 in Healthy Participants

NCT05492201 ↗

Phase 1 Completed 84 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindBasic science

Summary

The main purpose of this study is to evaluate the safety and tolerability of LY3873862 when administered either in single or multiple doses in healthy participants. The study will also assess how fast LY3873862 gets into the blood stream and how long it takes the body to remove it. The study is open to healthy participants. The study will last up to approximately 58, 72, and 72 days for Part A, B, and C, respectively.

Timeline

Start
2022-08-11
Primary completion
2025-04-29
Completion
2025-04-29

Drugs

EvaluationDrugModalityDoseRoute
Subject LY3873862 Unknown — Oral

Indications

No indication recorded.