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A Relative Bioavailability Study of LY3454738 in Healthy Participants

Healthy Clinical Trial

Official title:
A Phase 1, Open-Label Study to Determine the Relative Bioavailability of LY3454738 in Healthy Participants

Clinical Trial Summary

The main purpose of this study is to look at the amount of the study drug, LY3454738 that gets into the blood stream and how long it takes the body to get rid of it when given under the skin comparing a test formulation versus a reference formulation in healthy participants. The study will also evaluate the safety and tolerability of LY3454738 and information about any side effects experienced will be collected. For each participant, the total duration of the study will be approximately up to 17 weeks, including screening period.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06173895
Study type Interventional
Source Eli Lilly and Company
Contact
Status Completed
Phase Phase 1
Start date January 12, 2024
Completion date May 2, 2024
View Details
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