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Active, not recruiting Phase 3 Interventional

Effect of Retatrutide Compared With Placebo in Participants With Type 2 Diabetes and Moderate or Severe Renal Impairment, With Inadequate Glycemic Control on Basal Insulin, With or Without Metformin and/or SGLT2 Inhibitor (TRANSCEND-T2D-3)

ClinicalTrials.gov ID: NCT06297603

Public ClinicalTrials.gov record NCT06297603. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 26, 2026, 6:21 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Randomized, Multicenter, Double-Blind Study to Investigate the Efficacy and Safety of Retatrutide Once Weekly Compared With Placebo in Adult Participants With Type 2 Diabetes, Moderate or Severe Renal Impairment With Inadequate Glycemic Control on Basal Insulin With or Without Metformin and/or SGLT2 Inhibitor

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to investigate the efficacy and safety of retatrutide compared with placebo in participants with Type 2 Diabetes and renal impairment, with inadequate glycemic control on basal insulin alone or a combination of basal insulin with or without metformin and/or sodium-glucose cotransporter-2 (SGLT2) inhibitor. The study will last about 14 months and may include up to 22 visits.

Study identification

NCT ID
NCT06297603
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Eli Lilly and Company
Industry
Enrollment
320 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 15, 2024 (Actual)
Primary completion
Oct 2026 (Estimated)
Completion
Nov 2026 (Estimated)
Last update posted
Jul 20, 2026

2024 – 2026

United States locations

U.S. sites
28
U.S. states
16
U.S. cities
27
Facility City State ZIP Site status
Nephrology Consultants Huntsville Alabama 35805 —
Clinical Research Institute of Arizona (CRI) - Sun City West Sun City West Arizona 85375 —
Kidney & Hypertension Center - Apple Valley Apple Valley California 92307 —
Hope Clinical Research, Inc. Canoga Park California 91303 —
Neighborhood Healthcare Institute of Health Escondido California 92025 —
EndoTrials Center for Clinical Research La Mesa California 91942 —
UCLA South Bay Endocrinology Torrance California 90505 —
Northeast Research Institute (NERI) Fleming Island Florida 32003 —
Encore Medical Research - Weston Weston Florida 33331 —
Orita Clinical Research Decatur Georgia 30034 —
CARE Institute Idaho Falls Idaho 83404 —
Cotton O'Neil Diabetes & Endocrinology Topeka Kansas 66606 —
Billings Clinic Billings Montana 59101 —
Excel Clinical Research, LLC Las Vegas Nevada 89109 —
Albany Medical College, Division of Community Endocrinology Albany New York 12203 —
NYC Research INC Long Island City New York 11106 —
Research Foundation of SUNY - University of Buffalo Williamsville New York 14221 —
University of North Carolina Medical Center Chapel Hill North Carolina 27514 —
Central States Research Tulsa Oklahoma 74136 —
Preferred Primary Care Physicians, Preferred Clinical Research-St. Clair Pittsburgh Pennsylvania 15243 —
AM Diabetes & Endocrinology Center Bartlett Tennessee 38133 —
Velocity Clinical Research, Dallas Dallas Texas 75230 —
Prime Revival Research Institute, LLC Flower Mound Texas 75098 —
Juno Research Houston Texas 77040 —
PlanIt Research, PLLC Houston Texas 77079 —
Southern Endocrinology Associates Mesquite Texas 75149 —
Texas Valley Clinical Research Weslaco Texas 78596 —
Diabetes & Endocrine Treatment Specialists Sandy City Utah 84093 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 48 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06297603, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 20, 2026 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06297603 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →