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The impact of early application of ricalizumab in patients with extremely high-risk ASCVD( atherosclerotic cardiovascular disease) after PCI (percutaneous coronary intervention) on blood lipids and inflammatory cytokines

The impact of early application of ricalizumab in patients with extremely high-risk ASCVD( atherosclerotic cardiovascular disease) after PCI (percutaneous coronary intervention) on blood lipids and inflammatory cytokines

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125281
Enrollment
Unknown
Registered
2026-05-25
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Extremely high-risk atherosclerotic cardiovascular disease

Interventions

control group 1:Statin drugs for lipid-lowering treatment
control group 2:Statins combined with ivoosumab for lipid-lowering treatment
research group:Statins combined with racleciximab for lipid-lowering treatment

Sponsors

The Yunnan South Central Hospital (The First People’s Hospital of Honghe Prefecture)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. There have been 2 or more severe ASCVD events; 2. There has been 1 or more ASCVD events and at the same time, 2 or more high-risk factors are present; 3. Severe ASCVD events include: (1) Acute Coronary Syndrome (ACS) occurred within the previous 12 months; (2) History of myocardial infarction (more than 12 months); (3) History of ischemic stroke; (4) Symptomatic peripheral vascular disease, which has received blood flow reconstruction or amputation in the past. 4. High-risk factors include: (1) Multivessel disease (coronary artery, cerebral artery, and peripheral artery with 2-3 ischemic symptoms of arterial lesions simultaneously); (2) Early-onset coronary heart disease (male onset age 4.9 mmol/L; (4) Previously received coronary artery bypass grafting or PCI treatment; (5) Diabetes; (6) Hypertension; (7) Chronic kidney disease (CKD) stage 3-4; (8) Smoking; (9) After the maximum tolerated dose of statin treatment, LDL-C is monitored = 2.6 mmol/L.

Exclusion criteria

Exclusion criteria: 1. Severe liver dysfunction: Alanine aminotransferase (ALT) > 3 times the normal upper limit or having active liver disease; 2. Currently participating in other clinical trials; 3. Had a history of infection within the past two weeks; 4. Has contraindications or intolerance to the drugs used in this study; 5. Has a mental disorder and cannot cooperate with treatment; 6. Renal dysfunction.

Design outcomes

Primary

MeasureTime frame
blood glucose;total cholesterol;lipoprotein-associated phospholipase A2;Lipoprotein a;C-reactive protein;interleukin-6;

Countries

China

Contacts

Public ContactTao Ma

The Yunnan South Central Hospital (The First People’s Hospital of Honghe Prefecture)

qianmengjiao@sina.com+86 150 8730 4927

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026