To Compare the Efficacy and Safety of HRS9531 and Placebo in Subjects With Overweight or Obese

NCT ID: NCT06396429

Last Updated: 2025-07-11

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE3
• Total Enrollment: 567 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-05-13
• Study Completion Date: 2025-07-07

Brief Summary

The study aims to evaluate the efficacy and safety of HRS9531 in subjects with overweight or obese for 48 weeks.

Conditions

Overweight or Obesity

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Treatment group A: HRS9531 injection

Group Type: EXPERIMENTAL

HRS9531 injection

Intervention Type: DRUG

HRS9531 injection; low dose

Treatment group B: HRS9531 injection

Group Type: EXPERIMENTAL

HRS9531 injection

Intervention Type: DRUG

HRS9531 injection; medium dose

Treatment group C: HRS9531 injection

Group Type: EXPERIMENTAL

HRS9531 injection

Intervention Type: DRUG

HRS9531 injection, high dose

Placebo injection

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

blank preparation, participants received matching placebo.

Interventions

HRS9531 injection

HRS9531 injection; low dose

Intervention Type: DRUG

HRS9531 injection

HRS9531 injection; medium dose

Intervention Type: DRUG

HRS9531 injection

HRS9531 injection, high dose

Intervention Type: DRUG

Placebo

blank preparation, participants received matching placebo.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Able and willing to provide a written informed consent.

2. Male or female subjects, ≥18 years of age at the time of signing informed consent.

3. At screening visit, BMI≥28.0 Kg/m2, or ≥24 Kg/m2 with at least one weight-related complication, such as prediabetes, hypertension, dyslipidemia, obstructive sleep apnea, and nonalcoholic fatty liver disease.

4. Diet and exercise control for at least 3 months before screening visit, and less than 5 kg self-reported change within the last 3 months.

5. Fertile male and female subjects (including partners) have no plans to have children and agree to use effective contraception within 2 months after signing the informed consent form and the last medication, and fertile female or male subjects have no plans to donate eggs/sperm; Fertile female subjects tested negative for regnancy within the first 3 days of randomization and were not lactating.

Exclusion Criteria

1. Presence of clinically significant lab results at screening visit;

2. Uncontrollable hypertension;

3. PHQ-9 score ≥15;

4. Medical history or illness that affects your weight;

5. History of diabetes;

6. Acute infection, acute trauma, or medium to large surgery within 1 month prior to screening;

7. History of acute cardiovascular and cerebrovascular diseases within 6 months prior to screening;

8. Any organ-system malignancies developed within 5 years except for cured local basal cell cancer of the skin、 in-situ cancer of the cervix and in-situ cancer of the prostate;

9. Confirmed or suspected depression, bipolar disorder, suicidal tendencies, schizophrenia, or other serious mental illness;

10. Known or suspected history of alcohol and/or substance abuse or drug abuse;

11. History of acute or chronic hepatitis or other serious liver disease other than alcoholic fatty liver disease.

12. Have received or plan to have an organ or bone marrow transplant during the study.

13. The presence of any blood disorders that may interfere with HbA1c testing.

14. Autoimmune disease is present and systemic glucocorticoid therapy or immunosuppressive therapy is planned during the study.

15. Use of drugs or treatments that may have caused significant weight gain or loss within the 3 months prior to screening;

16. Weight loss surgery or endoscopic and/or medical device-based weight loss therapy is planned for or during the study period;

17. Use of drugs or treatments that may have caused significant weight gain or loss within the 3 months prior to screening;

18. Patients with blood donation or blood loss ≥400 mL or receiving blood transfusion within 3 months before screening.

19. Surgery is planned during the tria;

20. Mentally incapacitated or speech-impaired subjects are unable to fully understand or participate in the test process；

21. In the investigator's judgment, there are circumstances (medical, psychological, social, or geographical factors, etc.) that affect subject safety or any other conditions that interfere with the evaluation of the test results.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Fujian Shengdi Pharmaceutical Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Zhongshan Hospital Affiliated to Fudan University

Shanghai, Shanghai Municipality, China

Countries

China

Other Identifiers

HRS9531-301

Identifier Type: -

Identifier Source: org_study_id