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A Research Study Looking at Similarity Between LY3437943 Versions for Different Injection Devices

Healthy Clinical Trial

Official title:
A Relative Bioavailability Study to Compare the Pharmacokinetics of LY3437943 Administered Subcutaneously by a Test Device (Test Formulation) Versus Reference Device (Reference Formulation) in Healthy Participants

Clinical Trial Summary

The main purpose of this study is to look at the amount of the study drug, LY3437943, that gets into the blood stream and how long it takes the body to get rid of it when given using two different devices. The study will also evaluate the safety and tolerability of LY3437943 and information about any side effects experienced will be collected. For each participant, the total duration of the study will be approximately 16 weeks, including screening.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06003465
Study type Interventional
Source Eli Lilly and Company
Contact
Status Completed
Phase Phase 1
Start date August 29, 2023
Completion date February 8, 2024
View Details
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