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A Study to Compare Two Formulations of LY3819469 in Healthy Participants

Healthy Clinical Trial

Official title:
A Single Dose Study to Assess the Pharmacokinetics of 2 Formulations of LY3819469 in Healthy Participants

Clinical Trial Summary

The main purpose of this study is to assess two formulations of LY3819469 based on the amount that gets into the blood stream and how long it takes the body to get rid of it, when given to healthy participants. The information about any adverse effects experienced will be collected and the tolerability of LY3819469 will also be evaluated. Screening is required within 28 days prior to the enrolment. For each participant, the total duration of the clinical trial will be about 17 weeks including screening and follow-up periods.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05932446
Study type Interventional
Source Eli Lilly and Company
Contact
Status Completed
Phase Phase 1
Start date June 30, 2023
Completion date November 7, 2023
View Details
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