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RecruitingType 2 Diabetes

A Study of LY3457263 Compared With Placebo in Participants With Type 2 Diabetes on a Stable Dose of Semaglutide or Tirzepatide

Eligible age

18–75 yrs

Accepts

All genders

Locations

14 states

Healthy volunteers

No

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About this study

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.

Sponsor: Eli Lilly and Company

You may qualify if…

  • 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)

You may not qualify if…

  • 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)
  • unstable angina, or
  • hospitalization due to congestive heart failure
  • Have used insulin to control blood glucose within the past year (short-term use allowed)

Where it's recruiting

Arizona

Phoenix

California

Santa Ana

Florida

Ocala · Oviedo

Georgia

Lawrenceville · Union City · Woodstock

Idaho

Rexburg

Indiana

Brownsburg

New Jersey

Pennington

New York

Long Island City · Staten Island · West Seneca

North Carolina

Morehead City · Shelby

Ohio

Dayton

Oklahoma

Norman

Pennsylvania

Scottdale

Source: ClinicalTrials.gov · NCT06897475 · last updated 2026-06-23

A Study of LY3457263 Compared With Placebo in Participants With Type 2 · TrialPath