drugset / Trial / NCT05444569

A Study of LY3537021 in Healthy Participants

NCT05444569

Phase 1 Completed 47 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindBasic science

Summary

The main purpose of this study is to evaluate the safety and tolerability of LY3537021 when administered in combination with glucagon-like peptide (GLP-1) receptor agonist called liraglutide in treatment-naïve healthy participants. The study will include 2 parts. The study will last up to 16 and 22 weeks for part A and B, respectively which includes a screening period of 6 weeks.

Timeline

Start
2022-08-08
Primary completion
2023-02-24
Completion
2023-02-24

Drugs

EvaluationDrugModalityDoseRoute
Subject LY3537021 Unknown Subcutaneous
Background Liraglutide Peptide Subcutaneous

Indications

No indication recorded.