A Study of Tirzepatide (LY3298176) in Participants With Overweight or Obesity and Chronic Kidney Disease With or Without Type 2 Diabetes
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.
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:
- Have a Body Mass Index (BMI) ≥27 kilogram/square meter (kg/m²) at screening
- Diagnosed with chronic kidney disease (CKD)
- 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)
- 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:
- Have been diagnosed at least 180 days prior to screening
- Have HbA1c ≤9.5% at screening
EXCLUSION CRITERIA
Exclusion Criteria:
All participants:
- Have a self-reported change in body weight >5 kilogram (kg) within 90 days prior to screening.
- Have a prior or planned surgical treatment for obesity
- Have or plan to have endoscopic and/or device-based therapy for obesity or have had device removal within the last 180 days
- 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.
- Have a history of unstable or rapidly progressing renal disease according to investigator judgment
- 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)
- Have had a history of chronic or acute pancreatitis
Participants with T2D:
- Have history of proliferative diabetic retinopathy or diabetic macular edema or non-proliferative diabetic retinopathy that requires acute treatment.
- Have been diagnosed with type 1 diabetes (T1D) or have history of ketoacidosis or hyperosmolar state/coma
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
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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