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Not yet recruiting Phase 3 NCT07551492

A Phase III Study To Evaluate the Efficacy And Safety Of HRS9531 In Participants With Atherosclerotic Cardiovascular Disease

Phase 3 – large-scale trial before approval
Conditions: Atherosclerotic Cardiovascular Disease

Sponsor: Fujian Shengdi Pharmaceutical Co., Ltd.

trial.available_in: БГ
Overview
The purpose of the study is to evaluate the impact of HRS9531 on major adverse cardiovascular events (MACE) in patients with atherosclerotic cardiovascular disease. This study adopts an event-driven design and ends when the target number of the primary endpoint event is reached.
Who can participate
Inclusion Criteria: 1. Diagnosed with atherosclerotic cardiovascular disease (ASCVD), and the course of the disease exceeds 3 months 2. The body mass index (BMI) at the time of screening was ≥24.0 kg/m ². Patients with type 2 diabetes have a BMI of ≥22.0 kg/m ² Exclusion Criteria: 1. Screening for myocardial infarction, acute decompensated heart failure, hospitalization due to heart failure, unstable angina pectoris, stroke or transient ischemic attack, coronary revascularization, atrial flutter/fibrillation ablation, valve repair/replacement, carotid or peripheral artery recanalization within 30 days prior to the screening 2. Severe hypoglycemic events or recurrent hypoglycemic events occurred within one month before screening 3. When screening, there are proliferative retinopathy or macular degeneration requiring acute treatment, painful diabetic neuropathy, diabetic foot ulcers, and intermittent claudication 4. Coronary revascularization, atrial flutter/fibrillation ablation, valve repair/replacement, and carotid or peripheral artery recanalization are planned to be performed during the trial 5. Those with a history of acute or chronic pancreatitis, acute cholecystitis, or symptomatic or treatment-requiring gallbladder diseases 6. Any malignant tumor of the organ system has occurred within the past five years, regardless of whether there is evidence of local recurrence or metastasis, except for cured local cutaneous basal cell carcinoma and cervical carcinoma in situ 7. Pregnant or lactating women, or participants with fertility who are unwilling to take effective contraceptive measures 8. Those who have had any previous conditions that affected gastric emptying or have undergone gastrointestinal surgery 9. Diagnosed or suspected as type 1 diabetes, special type diabetes or secondary diabetes 10. Acute complications of diabetes occurred within one month before screening 11. There are endocrine diseases that may significantly affect weight
Interventions
HRS9531
DRUG
HRS9531 placebo
DRUG
Locations 1
China (1)
Fuwai Hospital, CAMS&PUMC
Beijing , Beijing Municipality
Technical details
Status
Not yet recruiting
Phase
Phase 3
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
01.05.2026
Completion date
01.06.2031
Registry ID
NCT07551492
Source
clinicaltrials.gov
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