For Healthcare Professionals

A Study of Tirzepatide (LY3298176) in Participants With Overweight or Obesity and Chronic Kidney Disease With or Without Type 2 Diabetes

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About the study

We are doing this study to learn more about how tirzepatide may help fight chronic kidney disease in people with obesity with or without type 2 diabetes (T2D). The study will last about 56 weeks and include up to 12 visits.
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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:


All participants with or without diabetes:


  1. Have a Body Mass Index (BMI) ≥27 kilogram/square meter (kg/m²) at screening
  2. Diagnosed with chronic kidney disease (CKD)
  3. Has an estimated glomerular filtration rate (eGFR) ≥25 to ≤60 ml/min/1.73 m² or eGFR ≥25 to ≤75 ml/min/1.73 m² if urine albumin-to-creatinine ratio (UACR) >30 milligram/gram (mg/g)
  4. Have been receiving an angiotensin-converting enzyme (ACE) or angiotensin II receptor blockers (ARB) that is considered the maximal appropriate dose by the investigator for treatment of chronic kidney disease or hypertension (unless the participant has low blood pressure or hypotension)

Participants without diabetes:


* Have Hemoglobin A1c (HbA1c) <6.5% at screening


Participants with Type 2 diabetes:


  1. Have been diagnosed at least 180 days prior to screening
  2. Have HbA1c ≤9.5% at screening

EXCLUSION CRITERIA

Exclusion Criteria:


All participants:


  1. Have a self-reported change in body weight >5 kilogram (kg) within 90 days prior to screening.
  2. Have a prior or planned surgical treatment for obesity
  3. Have or plan to have endoscopic and/or device-based therapy for obesity or have had device removal within the last 180 days
  4. Have eGFR <25 mL/min/1.73m² calculated by using creatinine-based chronic kidney disease epidemiology collaboration (CKD-EPI) equations, as determined by central laboratory at screening.
  5. Have a history of unstable or rapidly progressing renal disease according to investigator judgment
  6. Have a known clinically significant gastric emptying abnormality (for example, severe diabetic gastroparesis or gastric outlet obstruction) or chronically take drugs that directly affect GI motility)
  7. Have had a history of chronic or acute pancreatitis

Participants with T2D:


  1. Have history of proliferative diabetic retinopathy or diabetic macular edema or non-proliferative diabetic retinopathy that requires acute treatment.
  2. Have been diagnosed with type 1 diabetes (T1D) or have history of ketoacidosis or hyperosmolar state/coma

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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

Overweight,Obesity,Chronic Kidney Disease,Type 2 Diabetes,T2D

Age

18+

Phase

PHASE2

Participants Needed

140

Est. Completion Date

Feb 28, 2026

Treatment Type

INTERVENTIONAL


Sponsor

Eli Lilly and Company

ClinicalTrials.gov NCT Identifier

NCT05536804

Study Number

I8F-MC-GPIG

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