For Healthcare Professionals

A Study of Investigational Tirzepatide (LY3298176) Doses in Participants With Type 2 Diabetes and Obesity

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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.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria

  1. Have a Body Mass Index (BMI) ≥35 kilogram/square meter (kg/m²) at screening.
  2. Have had stable body weight (±5%) during the 90 days preceding screening.
  3. Have been diagnosed with Type 2 Diabetes (T2D).
  4. 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:

  1. Have Type 1 Diabetes (T1D), history of ketoacidosis or hyperosmolar state/coma, or any other types of diabetes except T2D.
  2. Have had 1 or more episode of severe hypoglycemia and/or 1 or more episode of hypoglycemia unawareness within 6 months prior to screening.
  3. Are currently receiving or planning to receive treatment for diabetic retinopathy and/or macular edema.
  4. Have a prior or planned surgical treatment for obesity.
  5. Use products intended for weight loss including prescription drugs, over the counter (OTC) drugs, and herbal preparations, within 3 months prior to screening.
  6. Have renal impairment measured as estimated glomerular filtration rate (eGFR) <45 milliliter/min (mL/min)/1.73 m².
  7. Have any of the following cardiovascular (CV) conditions within 2 months prior to screening.
  1. acute myocardial infarction.
  2. cerebrovascular accident (stroke).
  3. unstable angina .
  4. hospitalization due to congestive heart failure, or
  5. coronary artery revascularization.
  6. Have a family or personal history of medullary thyroid carcinoma or multiple endocrine neoplasia (MEN) syndrome Type 2.
  7. Have a history of chronic or acute pancreatitis.
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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.
Phone iconCall 1-317-615-4559Email iconEmail Study Center

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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