GLPwatch

Efficacy and Safety of Triple Therapy With Dulaglutide, SGLT2 Inhibitors, and Finerenone in Chinese Adults With Type 2 Diabetes and Chronic Kidney Disease

NCT07537088 · Not yet recruiting

Last updated 2026-05-28

This clinical trial is testing a combination of three medications (dulaglutide, SGLT2 inhibitors, and finerenone) in Chinese adults with type 2 diabetes and chronic kidney disease to evaluate their effects on kidney health.

Status Not yet recruiting Approved but enrollment has not started.
Phase Phase 4 Monitors a drug already on the market.
Type Interventional (clinical trial)
Design Randomized, open-label (no blinding) treatment study
Participants 468 people Planned (estimated).
Who can join Ages 18+ · all sexes
Timeline Started 2026-05 · est. completion 2027-07

What this study is testing ClinicalTrials.gov NCT07537088 ↗

Description as written by the study sponsor.

The purpose of this study is to evaluate whether adding dulaglutide to the combination therapy of Sodium-Glucose Co-Transporter 2 Inhibitors(SGLT2i) and finerenone can provide additional kidney protection and safety for Chinese adults with Type 2 Diabetes Mellitus(T2DM) and Chronic Kidney Disease(CKD). Eligible participants will be adults with T2DM and mild-to-moderate CKD who have been receiving SGLT2 inhibitor plus finerenone for at least 3 months on the basis of maximum tolerated dose of renin-angiotensin system inhibitor (RASi). Participants will be randomly assigned to either continue the original regimen or to receive add-on therapy with dulaglutide.The study will last for 26 weeks, with participants required to attend scheduled visits for efficacy and safety assessments at Week 13 (±1 week) and Week 26 (±1 week, final visit).

Treatments tested

Main thing measuredUrine Albumin-to-Creatinine Ratio(UACR)
SponsorFirst Affiliated Hospital of Wannan Medical College
Conditions studiedT2DM (Type 2 Diabetes Mellitus), CKD - Chronic Kidney Disease
GLP-1 drugs dulaglutide

Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT07537088 ↗