A Study of Investigational Tirzepatide (LY3298176) Doses in Participants With Type 2 Diabetes and Obesity
About the study
The main purpose of this study is to learn more about the safety and efficacy of investigational tirzepatide doses in participants with Type 2 diabetes and obesity that are already taking metformin. The study will last for about 89 weeks.
Who can take part
You may be eligible to participate in the study if you meet the following criteria:
INCLUSION CRITERIA
Inclusion Criteria
- Have a Body Mass Index (BMI) ≥35 kilogram/square meter (kg/m²) at screening.
- Have had stable body weight (±5%) during the 90 days preceding screening.
- Have been diagnosed with Type 2 Diabetes (T2D).
- Have been on a stable treatment of metformin only at least 90 days preceding screening and between screening and randomization with the minimum effective dose of ≥1500 milligram (mg)/day.
EXCLUSION CRITERIA
Exclusion Criteria:
- Have Type 1 Diabetes (T1D), history of ketoacidosis or hyperosmolar state/coma, or any other types of diabetes except T2D.
- Have had 1 or more episode of severe hypoglycemia and/or 1 or more episode of hypoglycemia unawareness within 6 months prior to screening.
- Are currently receiving or planning to receive treatment for diabetic retinopathy and/or macular edema.
- Have a prior or planned surgical treatment for obesity.
- Use products intended for weight loss including prescription drugs, over the counter (OTC) drugs, and herbal preparations, within 3 months prior to screening.
- Have renal impairment measured as estimated glomerular filtration rate (eGFR) <45 milliliter/min (mL/min)/1.73 m².
- Have any of the following cardiovascular (CV) conditions within 2 months prior to screening.
- acute myocardial infarction.
- cerebrovascular accident (stroke).
- unstable angina .
- hospitalization due to congestive heart failure, or
- coronary artery revascularization.
- Have a family or personal history of medullary thyroid carcinoma or multiple endocrine neoplasia (MEN) syndrome Type 2.
- Have a history of chronic or acute pancreatitis.
Study Locations
Enter your ZIP code/Postal code/PIN code to locate study sites near you:
How to Apply
Contact the study center to learn if this study is a good match for you.
Study Details
Contition
Type 2 Diabetes,Obesity
Age
18 - 75
Phase
PHASE2
Participants Needed
350
Est. Completion Date
Oct 31, 2026
Treatment Type
INTERVENTIONAL
Sponsor
Eli Lilly and Company
ClinicalTrials.gov NCT Identifier
NCT06037252
Study Number
I8F-MC-GPIT
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