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A Study of LY3457263 Compared With Placebo in Participants With Type 2 Diabetes on a Stabl

The purpose of this study is to measure the change in hemoglobin A1c (HbA1c) with LY3457263 compared with placebo in participants with type 2 diabetes who are not at HbA1c goal when treated with a stable dose of semaglutide or tirzepatide. Participation in the study will last about 9 months.

Condition(s)Type 2 Diabetes
StatusRecruiting
PhasePhase 2
Study typeInterventional
SummaryThe purpose of this study is to measure the change in hemoglobin A1c (HbA1c) with LY3457263 compared with placebo in participants with type 2 diabetes who are not at HbA1c goal when treated with a stable dose of semaglutide or tirzepatide. Participation in the study will last about 9 months.
Who can participateInclusion Criteria: * Have type 2 diabetes * Have HbA1c ≥7.5% to ≤10.5% at screening * Have a body mass index (BMI) of ≥27 kilograms per square meter (kg/m2) at screening * Have had a stable body weight for the three months prior to screening * On stable treatment dose of one of the following incretins for at least three months prior to screening: * Injectable semaglutide (1 and 2 milligram (mg)) * Injectable tirzepatide (5, 7.5, 10, 12.5 and 15 mg) Exclusion Criteria: * Have type 1 diabetes, latent autoimmune diabetes, or history of ketoacidosis or hyperosmolar coma * Have a prior or planned surgical treatment for obesity * Have any of the following cardiovascular conditions within three months prior to screening: * acute myocardial infarction * cerebrovascular accident (stroke) * unstabl
Ages18 Years to 75 Years
SexAll
Lead sponsorEli Lilly and Company
LocationsPhoenix, Arizona, United States; Santa Ana, California, United States; Ocala, Florida, United States; Oviedo, Florida, United States; Lawrenceville, Georgia, United States; Lawrenceville, Georgia, United States (+54 more sites)
Start date2025-03-28
NCT IDNCT06897475
Official listinghttps://clinicaltrials.gov/study/NCT06897475

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