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NCT05936151CompletedPhase 2

A Study of Retatrutide (LY3437943) on Renal Function in Participants With Overweight or Obesity and Chronic Kidney Disease With or Without Type 2 Diabetes

A Phase 2b, Double-Blind Study to Investigate the Effect of Retatrutide on Renal Function in Participants With Overweight or Obesity and Chronic Kidney Disease With or Without Type 2 Diabetes

Source: ClinicalTrials.gov · Last updated 25 Nov 2025

Brief summary (registry, in English)

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 last around 31 weeks.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
146 (actual)
First submitted
30 Jun 2023
Start date
20 Jul 2023
Primary completion date
1 Oct 2025
Lead sponsor
Eli Lilly and Company
NCT number
NCT05936151
EU CT number
2023-504583-42-00

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 146
  • From 20 Jul 2023 to the primary completion date, 1 Oct 2025
  • 42 sites in 5 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • 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

Other illness

  • Have Type 1 Diabetes (T1D)
  • Have acute or chronic hepatitis
  • Have a history of malignant disease within 5 years before screening.

Who the study is looking for

  • 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).

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (42)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Centricity Research Brampton Endocrinology
Coordinator of this site? Confirm its status
BramptonCanadaUnknown status
Circulate Cardiac & Vascular Centre
Coordinator of this site? Confirm its status
BurlingtonCanadaUnknown status
Viacar Recherche Clinique
Coordinator of this site? Confirm its status
Greenfield ParkCanadaUnknown status
Diex Recherche (Joliette)
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JolietteCanadaUnknown status
9109-0126 Quebec Inc.
Coordinator of this site? Confirm its status
MontrealCanadaUnknown status
North York Diagnostic and Cardiac Centre
Coordinator of this site? Confirm its status
North YorkCanadaUnknown status
Stouffville Medical Research Institute Inc.
Coordinator of this site? Confirm its status
StouffvilleCanadaUnknown status
Dr. Anil K. Gupta Medicine Professional Corporation
Coordinator of this site? Confirm its status
TorontoCanadaUnknown status
Fadia El Boreky Medicine
Coordinator of this site? Confirm its status
WaterlooCanadaUnknown status
Nuevas Tecnologias En Diabetes Y En Endocrinologia S.L. Profesional
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SevillaSpainCompleted
Hospital Clinico Universitario de Valencia
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ValenciaSpainCompleted
Hospital Universitario Dr. Peset Aleixandre
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ValenciaSpainCompleted
Addenbrooke's Hospital
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CambridgeUnited KingdomUnknown status
North Middlesex Hospital
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LondonUnited KingdomUnknown status
Royal London Hospital
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LondonUnited KingdomUnknown status
Futuremeds-Newcastle
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NewcastleUnited KingdomUnknown status
City Hospital, Nottingham University Hospitals NHS Trust
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NottinghamUnited KingdomUnknown status
Vascular Research Team
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SalfordUnited KingdomUnknown status
FutureMeds Teesside - Middlefield Centre
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Stockton-on-TeesUnited KingdomUnknown status
Azienda Ospedaliera Papa Giovanni XXIII
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BergamoItalyCompleted
Centro Cardiologico Monzino S.p.A.
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MilanItalyCompleted
Ospedale San Raffaele S.r.l.
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MilanItalyCompleted
Azienda Ospedaliero Universitaria Pisana
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PisaItalyCompleted
University of Colorado Anschutz Medical Campus
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AuroraUnited StatesUnknown status
Teradan Clinical trials LLC
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BrandonUnited StatesUnknown status
Hope Clinical Research, Inc.
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Canoga ParkUnited StatesUnknown status
The Institute for Liver Health II dba Arizona Clinical Trials - Mesa
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ChandlerUnited StatesUnknown status
Great Lakes Clinical Trials - Ravenswood
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ChicagoUnited StatesUnknown status
Cleveland Clinic
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ClevelandUnited StatesUnknown status
Prime Health and Wellness/SKYCRNG
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FayetteUnited StatesUnknown status
Victorium Clinical Research - Houston
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HoustonUnited StatesUnknown status
Endocrine Ips, Pllc
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HoustonUnited StatesUnknown status
Indiana University Health University Hospital
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IndianapolisUnited StatesUnknown status
Palm Research Center Tenaya
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Las VegasUnited StatesUnknown status
Care Access - 801 South Power Road, Mesa
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MesaUnited StatesUnknown status
NYU Langone Hospital - Long Island
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MineolaUnited StatesUnknown status
Catalina Research Institute, LLC
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MontclairUnited StatesUnknown status
Suncoast Clinical Research, Inc.
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New Port RicheyUnited StatesUnknown status
Peninsula Research Associates
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Rolling Hills EstatesUnited StatesUnknown status
Headlands Research - Scottsdale
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ScottsdaleUnited StatesUnknown status
Medical Advancement Centers of Arizona
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TempeUnited StatesUnknown status
Tranquility Research
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WebsterUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.