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Priya Life Science Compound trial record
Compound · clinical trials

HRS9531 clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 11 trials in our China register that name HRS9531 as an intervention. Synced 10 Nov 2026
11Current trials
7Recruiting now
1Lead sponsor
1Country register
At a glance

HRS9531 is named as an intervention in 11 current clinical trials in our China register. 7 are recruiting patients now. The most common phase is Phase 3. The lead sponsor is Fujian Shengdi Pharmaceutical Co., Ltd. The most-studied condition is Type 2 Diabetes.

Patient leaflets for HRS9531

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • UK
    United Kingdom: Search MHRA Products
    Patient information leaflets and SmPCs for UK-licensed products.
  • US
    United States: Search DailyMed
    FDA-approved labels, including patient and medication guides.

Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.

Trials by status

  • Recruiting764%
  • Not yet open19%
  • Active, closed327%

Trials by phase

  • Phase 3655%
  • Phase 2327%
  • Phase 1218%
01

Clinical trials of HRS9531

11 trials
StudyPhaseStatusLead sponsorRegisters
A Phase III Study Evaluating the Efficacy and Safety of HRS9531 Injection in Subjects With Obstructive Sleep Apnea (OSA) and Obesity
NCT06974851 · ClinicalTrials.gov ↗ · Bstructive Sleep Apnea (OSA) and Obesity
Phase 3 Recruiting Fujian Shengdi Pharmaceutical Co., Ltd China
Efficacy and Safety of HRS9531 in Participants With Type 2 Diabetes Treated With Basal Insulin
NCT07060456 · ClinicalTrials.gov ↗ · Type 2 Diabetes
Phase 3 Recruiting Fujian Shengdi Pharmaceutical Co., Ltd China
A Phase III Study To Evaluate the Efficacy And Safety Of HRS9531 In Participants With Atherosclerotic Cardiovascular Disease
NCT07551492 · ClinicalTrials.gov ↗ · Atherosclerotic Cardiovascular Disease
Phase 3 Recruiting Fujian Shengdi Pharmaceutical Co., Ltd China
A Clinical Study to Evaluate the Efficacy and Safety of HRS9531 Tablets in Overweight or Obese Subjects
NCT07670884 · ClinicalTrials.gov ↗ · Chronic Management of Body Weight
Phase 3 Recruiting Fujian Shengdi Pharmaceutical Co., Ltd China
A Research Study to Investigate the Efficacy and Safety of HRS9531 Tablets in Participants With Type 2 Diabetes Mellitus
NCT07599410 · ClinicalTrials.gov ↗ · T2DM
Phase 2 Recruiting Fujian Shengdi Pharmaceutical Co., Ltd China
A Study of HRS-4729 Injection and HRS9531 Injection in Participants With Metabolic Dysfunction-Associated Steatohepatitis
NCT07660848 · ClinicalTrials.gov ↗ · Metabolic Dysfunction-Associated Steatohepatitis (MASH)
Phase 2 Recruiting Fujian Shengdi Pharmaceutical Co., Ltd China
A Study to Evaluate the Pharmacokinetics of HRS9531 Injection in Participants With Mild, Moderate, and Normal Hepatic Function
NCT07540754 · ClinicalTrials.gov ↗ · Diabetes Mellitus, Weight Loss
Phase 1 Recruiting Fujian Shengdi Pharmaceutical Co., Ltd China
A Clinical Study to Evaluate the Effect of Different Dosing Conditions on the Pharmacokinetics of HRS9531 Tablets in Healthy Participants
NCT06506175 · ClinicalTrials.gov ↗ · Weight Management, Type 2 Diabetes
Phase 1 Not yet open Fujian Shengdi Pharmaceutical Co., Ltd China
A Multicenter, Randomized, Double-blind, Placebo-controlled Phase III Clinical Study to Evaluate the Efficacy and Safety of HRS9531 Injection in Subjects With Obstructive Sleep Apnea (OSA) and Obesity Who Are on Positive Airway Pressure Ventilation (PAP) Therapy
NCT06994650 · ClinicalTrials.gov ↗ · Subjects With Moderate-to-severe OSA and Obesity Who Are on PAP Therapy
Phase 3 Active, closed Fujian Shengdi Pharmaceutical Co., Ltd China
A Study Comparing the Efficacy and Safety of HRS9531 Injection With Semaglutide Injection in Subjects With Obesity
NCT07285902 · ClinicalTrials.gov ↗ · Obesity
Phase 3 Active, closed Fujian Shengdi Pharmaceutical Co., Ltd China
HRS9531 Injection in Obese Subjects With Heart Failure With Preserved Ejection Fraction
NCT06391710 · ClinicalTrials.gov ↗ · Heart Failure With Preserved Ejection Fraction
Phase 2 Active, closed Fujian Shengdi Pharmaceutical Co., Ltd China

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied with HRS9531

12 conditions
Type 2 Diabetes2T2DM1Subjects With Moderate-to-severe OSA and Obesity Who Are on PAP Therapy1Heart Failure With Preserved Ejection Fraction1Bstructive Sleep Apnea (OSA) and Obesity1Diabetes Mellitus1Weight Loss1Atherosclerotic Cardiovascular Disease1Metabolic Dysfunction-Associated Steatohepatitis (MASH)1Weight Management1Obesity1Chronic Management of Body Weight1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Fujian Shengdi Pharmaceutical Co., Ltd11
04

By country register

RegisterTrialsRecruiting
Clinical trials in China117

A trial with sites in more than one country appears in each of those registers.

05

Related compounds

06

Questions about HRS9531 trials

How many clinical trials are testing HRS9531?

11 current trials in our China register name HRS9531 as a drug or biological intervention, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.

Are HRS9531 trials recruiting patients?

Yes. 7 of the 11 trials are recruiting: 7 with sites in China. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors HRS9531 clinical trials?

The lead sponsor is Fujian Shengdi Pharmaceutical Co., Ltd. The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how HRS9531 works or whether it is effective, and it is not medical advice.

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How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how HRS9531 works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists HRS9531 (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 10 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.