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)
- Disease/Condition
- Type 2 Diabetes
- Drug/Device/Intervention
- Retatrutide
- Study type
- Interventional
- Intervention type
- drug
- Primary sponsor
- Eli Lilly and Company
- Location
- Sun City West,La Mesa,Torrance,Fleming Island,Idaho Falls,Topeka,Billings,Reno,Albany,Buffalo,Long Island City,Chapel Hill,Hickory,Cleveland,Tulsa,Pittsburgh,Bartlett,Dallas,Houston,Houston,Mesquite,S, Argentina,Puerto Rico,United Kingdom,United States of America
- Phase
- Phase 3
- Start date
- Mar 15, 2024
- End date
- Oct 09, 2026
- Enrollment
- 320 participants
Change from Baseline in Hemoglobin A1c (HbA1c) (%)
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.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06297603
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT06297603 through Pure Global AI's free database. This Phase 3 trial is sponsored by Eli Lilly and Company and is currently Recruiting. The study focuses on Type 2 Diabetes. Target enrollment is 320 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.