RecruitingPhase 2NCT07599410

A Research Study to Investigate the Efficacy and Safety of HRS9531 Tablets in Participants With Type 2 Diabetes Mellitus

A Multicenter, Randomized, Double Blind, Placebo Controlled, Parallel Group Phase 2 Study to Evaluate the Efficacy and Safety of HRS9531 Tablets in Participants With Type 2 Diabetes Mellitus.


Sponsor

Fujian Shengdi Pharmaceutical Co., Ltd.

Enrollment

240 participants

Start Date

Jul 14, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The aim of the trial is to investigate the efficacy and safety of HRS9531 tablets versus placebo in participants with type 2 diabetes mellitus who failed to achieve adequate glycemic control on lifestyle intervention alone or on a stable dose of metformin. This study will last 20 weeks.


Eligibility

Min Age: 18 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called HRS9531 Tablet, a drug called HRS9531 Tablet, and others for people with t2dm. The study is currently recruiting participants at 2 locations. People eligible for this study include aged 18 Years to 70 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGHRS9531 Tablet

HRS9531 Tablet dose 1

DRUGHRS9531 Tablet

HRS9531 Tablet dose 2

DRUGHRS9531 Tablet

HRS9531 Tablet dose 3

DRUGHRS9531 Tablet

HRS9531 Tablet dose 4

DRUGHRS9531 Tablet

HRS9531 Tablet dose 5

DRUGHRS9531 Tablet placebo

HRS9531 Tablet placebo


Locations(2)

Beijing Chaoyang Hospital, Capital Medical University

Beijing, Beijing Municipality, China

Qilu Hospital of Shandong University

Jinan, Shandong, China

View Full Details on ClinicalTrials.gov

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NCT07599410


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