Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT07537088

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

Efficacy and Safety of Dulaglutide, SGLT-2 Inhibitors, and Finerenone Triple Therapy in Chinese Adults With Type 2 Diabetes and Chronic Kidney Disease: A Multicenter, Prospective, Randomized Controlled Study

Status
Not Yet Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
468 (estimated)
Sponsor
First Affiliated Hospital of Wannan Medical College · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate whether adding dulaglutide to the combination therapy of SGLT2i and finerenone can provide additional kidney protection and safety for Chinese adults with T2DM and 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).

Conditions

Interventions

TypeNameDescription
DRUGDulaglutideDulaglutide 1.5 mg, once weekly
DRUGSGLT2iadministered according to prescribing information
DRUGFinerenoneadministered according to prescribing information

Timeline

Start date
2026-05-01
Primary completion
2027-04-01
Completion
2027-07-01
First posted
2026-04-17
Last updated
2026-04-17

Source: ClinicalTrials.gov record NCT07537088. Inclusion in this directory is not an endorsement.