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

Description

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.

Conditions

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

Study Overview

Study Details

Study overview

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.

Tirzepatide Study of Renal Function in People With Overweight or Obesity and Chronic Kidney Disease With or Without Type 2 Diabetes: Focus on Kidney Hypoxia in Relation to Fatty Kidney Disease Using Multiparametric Magnetic Resonance Imaging

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

Condition
Overweight
Intervention / Treatment

-

Contacts and Locations

Northridge

Valley Clinical Trials, Inc., Northridge, California, United States, 91325

Aurora

University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States, 80045

Denver

Kidney Associates of Colorado, Denver, Colorado, United States, 80210

Avon

American Health Network of Indiana, LLC - Avon, Avon, Indiana, United States, 46123

Greenfield

American Health Network of Indiana, LLC - Greenfield, Greenfield, Indiana, United States, 46140

Indianapolis

Indiana University Health University Hospital, Indianapolis, Indiana, United States, 46202

Muncie

American Health Network of Indiana, LLC - Muncie, Muncie, Indiana, United States, 47304

Troy

Arcturus Healthcare , PLC, Troy Internal Medicine Research Division, Troy, Michigan, United States, 48098

Seattle

University of Washington Medical Center - Montlake, Seattle, Washington, United States, 98195

Spokane

Providence Medical Research Center - Spokane, Spokane, Washington, United States, 99204

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * 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)
  • * Have Hemoglobin A1c (HbA1c) \<6.5% at screening
  • * Have been diagnosed at least 180 days prior to screening
  • * Have HbA1c ≤9.5% at screening
  • * 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
  • * 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

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Eli Lilly and Company,

Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST), STUDY_DIRECTOR, Eli Lilly and Company

Study Record Dates

2026-02