A Study of LY3532226 in Participants With Type 2 Diabetes Mellitus
NCT05407961 · Completed
Last updated 2026-05-28This clinical trial is testing the safety of the investigational drug LY3532226 in adults with type 2 diabetes.
Status Completed The study has finished.
Phase Phase 1 Checks safety and dosing in a small group.
Type Interventional (clinical trial)
Design Randomized, double-blind basic-science study
Participants 90 people
Who can join Ages 18–70 · all sexes
Timeline Started 2022-06 · est. completion 2024-01
Where 1 site · Germany
What this study is testing ClinicalTrials.gov NCT05407961 ↗
Description as written by the study sponsor.
The main purpose of this study is to evaluate the safety and tolerability of the study drug known as LY3532226 in participants with type 2 diabetes mellitus (T2DM). Blood tests will be performed to check how much LY3532226 gets into the bloodstream and how long it takes the body to eliminate it. This is a 2-part study and will last approximately 16 weeks excluding screening period for each part, respectively.
Treatments tested
- LY3532226 Drug
Administered SC.
- Placebo Drug
Administered SC.
- Dulaglutide also known as Trulicity Drug
Administered SC.
| Main thing measured | Part A: Number of Participants with One or More Treatment Emergent Adverse Events (TEAEs) and Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration |
|---|---|
| Sponsor | Eli Lilly and Company |
| Conditions studied | Diabetes Mellitus, Type 2 |
| GLP-1 drugs | — |
Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT05407961 ↗