drugset / Trial / NCT04682119

A Safety Study of LY3526318 in Healthy Participants

NCT04682119

Phase 1 Completed 16 enrolled Eli Lilly and Company
RandomizedSequentialDouble-blindBasic science

Summary

The main purpose of this study is to learn more about how the drug is absorbed in to the blood stream and how it is eliminated from the body. The safety and tolerability of LY3526318 will also be evaluated when given by mouth either by single or multiple doses to healthy participants. The study will have two parts. Each participant will enroll in only one part. For each participant, Part A will last up to 44 days and Part B will last up to 50 days, including screening and follow-up.

Timeline

Start
2020-12-29
Primary completion
2021-04-21
Completion
2021-04-21

Drugs

EvaluationDrugModalityDoseRoute
Subject LY3526318 Unknown 100 mg Oral
Subject LY3526318 Unknown 250 mg Oral

Indications

No indication recorded.