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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05936151
Other study ID # 18725
Secondary ID J1I-MC-GZBU2023-
Status Recruiting
Phase Phase 2
First received
Last updated
Start date July 20, 2023
Est. completion date November 25, 2025

Study information

Verified date April 2024
Source Eli Lilly and Company
Contact There may be multiple sites in this clinical trial. 1-877-CTLILL
Phone 1-317-615-4559
Email ClinicalTrials.gov@lilly.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The main purpose of this study is to investigate the effect of retatrutide on renal function in participants with overweight or obesity and chronic kidney disease (CKD), with or without Type 2 Diabetes (T2D). The study will lasts around 31 weeks.


Recruitment information / eligibility

Status Recruiting
Enrollment 120
Est. completion date November 25, 2025
Est. primary completion date November 25, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Have a body mass index (BMI) =27 kilogram/square meter (kg/m²) - Have either - no T2D with an HbA1c < 6.5% or - have T2D with an HbA1c = 9.5% and treated with diet and exercise only or with stable doses of up to 3 oral antihyperglycemic medications, with or without basal insulin for at least 90 days before screening. - Have been diagnosed with chronic kidney disease (CKD). Exclusion Criteria: - Have a self-reported change in body weight >5 kilogram (kg) (11 pounds) within 90 days before screening. - Have used in 90 days before the screening any of the following antihyperglycemic class: Dipeptidyl Peptidase IV (DPP4) inhibitors, amylin analogs, glucagon-like peptide-RA (GLP-RA), gastric inhibitory polypeptide (GIP)/GIP-1 RA, and short acting or rapid acting insulins or U500 Insulin - Have a prior or planned surgical treatment for obesity - Have Type 1 Diabetes (T1D) - Have acute or chronic hepatitis - Have a history of malignant disease within 5 years before screening.

Study Design


Intervention

Drug:
LY3437943
Administered SC
Placebo
Administered SC

Locations

Country Name City State
Canada Circulate Cardiac & Vascular Centre Burlington Ontario
Canada Viacar Recherche Clinique Greenfield Park Quebec
Canada 9109-0126 Quebec Inc. Montreal Quebec
Canada North York Diagnostic and Cardiac Centre North York Ontario
Canada Stouffville Medical Centre Stouffville Ontario
Canada Dr. Anil K. Gupta Medicine Professional Corporation Toronto Ontario
Canada Fadia El Boreky Medicine Waterloo Ontario
Italy Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII Bergamo
Italy Centro Cardiologico Monzino Milan Milano
Italy Ospedale San Raffaele Milano
Italy Azienda Ospedaliera Universitaria Pisana Pisa Toscana
Spain Clínica nuevas Tecnologías en Diabetes y Endocrinología (NTDE) Sevilla
Spain Hospital Clinico de Valencia Valencia Valenciana
Spain Hospital Universitario Doctor Peset Valencia Valenciana, Comunitat
United Kingdom Addenbrooke's Hospital Cambridge Cambridgeshire
United Kingdom North Middlesex Hospital London London, City Of
United Kingdom Royal London Hospital London England
United Kingdom City Hospital, Nottingham University Hospitals Nottingham
United Kingdom Vascular Research Team Salford Greater Manchester
United States University of Colorado Anschutz Medical Campus Aurora Colorado
United States Hope Clinical Research, Inc. Canoga Park California
United States Cleveland Clinic Cleveland Ohio
United States Endocrine Ips, Pllc Houston Texas
United States Victorium Clinical Research - Houston Houston Texas
United States Palm Research Center Tenaya Las Vegas Nevada
United States The Institute for Liver Health dba Arizona Clinical Trials Mesa Arizona
United States NYU Langone Hospital - Long Island Mineola New York
United States Catalina Research Institute, LLC Montclair California
United States Peninsula Research Associates Rolling Hills Estates California
United States Headlands Research - Scottsdale Scottsdale Arizona
United States Tranquility Research Webster Texas

Sponsors (1)

Lead Sponsor Collaborator
Eli Lilly and Company

Countries where clinical trial is conducted

United States,  Canada,  Italy,  Spain,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from Baseline in Glomerular Filtration Rate (GFR) The GFR in milliliter/minute/square meter (mL/min/m²) using iohexol clearance (mGFR-measured glomerular filtration rate) Baseline, Week 24
Secondary Change from Baseline in Urine Albumin-to-Creatinine Ratio (UACR) Baseline, Week 24
Secondary Change from Baseline in Creatinine-Corrected Fractional Urinary Sodium Excretion (FENa) Baseline, Week 24
Secondary Change from Baseline in Filtration Fraction Estimated from Measured Glomerular Filtration Rate (mGFR) Baseline, Week 24
Secondary Change from Baseline in Renal Mean Arterial Flow as Assessed by Magnetic Resonance Imaging (MRI), Corrected by Hematocrit Baseline, Week 24
Secondary Change from Baseline in in Mean Arterial Flow (MAF) Baseline, Week 24
Secondary Change from Baseline in Renal Artery Resistive Index (RARI) Baseline, Week 24
Secondary Change from Baseline in Renal Blood Flow Velocity Peak Systolic Velocity (PSV) and End-diastolic Velocity (ESV) Baseline, Week 24
Secondary Change from Baseline in Global Renal Perfusion (MRI) Baseline, Week 24
Secondary Change from Baseline in Total Renal Parenchyma Volume (MRI) Baseline, Week 24
Secondary Change from Baseline in Renal Cortex Volume (MRI) Baseline, Week 24
Secondary Change from Baseline in Renal Cortex T1 (ms) (MRI) Baseline, Week 24
Secondary Change from Baseline in Medulla T1 (ms) (MRI) Baseline, Week 24
Secondary Change from Baseline in Renal Cortex R2 (BOLD MRI) Baseline, Week 24
Secondary Change from Baseline in Medulla R2 Baseline, Week 24
Secondary Change from Baseline in Body Weight Baseline, Week 24
Secondary Change from Baseline in 24-hr Urinary Albumin Excretion (UAE) Baseline, Week 24
Secondary Change from Baseline in Change in 24-hour (hr) Urinary Electrolytes (milligrams/24hr (mg/24h)) Baseline, Week 24
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