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A Study of LY3875383 in Healthy Participants and Participants With Hypertriglyceridemia

Hypertriglyceridemia Clinical Trial

Official title:
A Single-Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LY3875383 in Healthy Participants and Participants With Hypertriglyceridemia

Clinical Trial Summary

The main purpose of this study is to determine the tolerability and side effects related to LY3875383 given as a single injection under the skin to healthy participants and participants with elevated triglyceride (TG) levels.The study will also assess how fast LY3875383 gets into the blood stream and how long the body takes to get rid of it. Each enrolled participant will receive a single dose of either LY3875383 or placebo.The study will be conducted in four parts (A, B, C and D) and may last up to approximately 28 to 56 weeks including screening.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05609825
Study type Interventional
Source Eli Lilly and Company
Contact
Status Completed
Phase Phase 1
Start date November 14, 2022
Completion date January 10, 2024
View Details
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