GLPwatch

Triple Hypoglycemic Regimens In Patients With Newly Diagnosed Type 2 Diabetes Mellitus

NCT07374328 · Recruiting

Last updated 2026-05-28

This clinical trial is testing three different combinations of diabetes medications in adults who were recently diagnosed with type 2 diabetes to see if any of the combinations help achieve diabetes remission.

Status Recruiting Currently enrolling participants.
Phase Phase1, Phase2
Type Interventional (clinical trial)
Design Randomized, single-blind treatment study
Participants 240 people Planned (estimated).
Who can join Ages 18–65 · all sexes
Timeline Started 2025-06 · est. completion 2026-08
Where 1 site · China

What this study is testing ClinicalTrials.gov NCT07374328 ↗

Description as written by the study sponsor.

This study is a multicenter, randomized, controlled study. A sample size of 240 cases is proposed to be included. The inclusion criteria are: (1) patients with newly diagnosed type 2 diabetes; (2) age between 18 and 65 years old; (3) HbA1c ≥ 9.0%. The exclusion criteria include: (1) type 1 diabetes; (2) elevated creatinine or urinary albumin/creatinine; (3) combined with coronary heart disease, tumor or pregnancy; (4) receiving glucocorticoids. The selected participants are randomly divided into two groups: one group is the semaglutide group, and the other isthe oral medication group. The treatment plan is as follows. Semaglutide group: 0.25 mg per week in the first month, 0.5 mg per week in the second month, and 1.0mg per week from the 3rd to the 8th month of semaglutide. Oral medication group: Sitagliptin 0.1g per day. Both groups were simultaneously treated with metformin (1.0g daily, divided into two doses) and empagliflozin (10mg daily). The first phase of the study was as follows: Semaglutide group: Treatment was initiated until 6 months after the titration dose of 1mg was reached; Oral medication group: Initiate treatment until 6 months after reaching a fixed dose. At the end of the first stage of the study, for the selected participants with HbA1c\<6.5%, the hypoglycemic drugs were discontinued and they entered the second stage of the study. The study was concluded after a 3-month follow-up. The evaluation indicators include: effectiveness indicators (HbA1c, diabetes remission rate, continuous glucose monitoring), safety indicators (hypoglycemia, adverse reactions, etc.).

Treatments tested

Main thing measuredDiabetes remission rate
SponsorSecond Affiliated Hospital of Guangzhou Medical University
Conditions studiedType 2 Diabetes
GLP-1 drugs

Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT07374328 ↗