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A First-In-Human Study of LY3839840 in Healthy Participants

Healthy Clinical Trial

Official title:
Single- and Multiple-Ascending Dose Study to Evaluate the Safety and Pharmacokinetics of LY3839840 Following Oral Dosing in Healthy Participants

Clinical Trial Summary

The main purpose of this first-in-human study to investigate the safety of LY3839840 in single and multiple doses, and how it's processed in the body when given in different amounts.

Clinical Trial Description

The study will be conducted in four parts (A, B, C and D) and each enrolled participant will receive a single dose (Parts A and C) or multiple dose (Parts B, C and D) of either LY3839840 or placebo. The study will last up to approximately 7 weeks for parts A, C (single dose cohort) and 8 weeks for parts B, D and C (multiple dose cohort). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06153355
Study type Interventional
Source Eli Lilly and Company
Contact There may be multiple sites in this clinical trial. 1-877-CTLILL
Phone 1-317-615-4559
Email ClinicalTrials.gov@Lilly.com
Status Recruiting
Phase Phase 1
Start date December 4, 2023
Completion date August 2024
View Details
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