A Study of LY3039478 in Healthy Participants

Completed · Phase 1 · Has a placebo group

Conditions studied: Healthy

In brief

The main purpose of this study is to investigate the safety of the study drug known as LY3039478 and evaluate two different formulations of LY3039478 in healthy participants. Part A has three periods. Either LY3039478 or placebo will be given once by mouth in each period. Part B has two periods. Participants will receive both formulations of LY3039478, by mouth, over the course of the study. Both parts of the study will also explore how much LY3039478 gets into the bloodstream and how long it takes the body to get rid of it. Information about any side effects will also be collected. Participants may only enroll in one part. The study will last at least 33 days, not including screening. Screening must be performed up to 30 days before enrollment. Part B was added by protocol amendment approved in April, 2016.

Key facts

Study ID

NCT02659865

Run by

Eli Lilly and Company

People needed

29

Starts

2016-01-01

Expected to finish

2016-06-01

Last updated by the study team

2025-08-12

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Body mass index (BMI) of 18 to 32 kilogram per meter square (kg/m²)

You may not qualify if…

• Known allergies to LY3039478, related compounds or any components of the formulation
• Have previously received LY3039478
• Smokers or who have stopped smoking less than 3 months prior to enrollment

Where it is running

• Covance — Daytona Beach, Florida, United States

Full record on ClinicalTrials.gov

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