Skip to content

Study of inclisiran to prevent cardiovascular events in participants with established cardiovascular disease

A Randomized, Double-blind, Placebo-controlled, Multicenter Trial, Assessing the Impact of Inclisiran on Major Adverse Cardiovascular Events in Participants With Established Cardiovascular Disease - VICTORION-2 PREVENT

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2031220634
Enrollment
36
Registered
2023-02-12
Start date
2023-04-12
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Atherosclerotic Cardiovascular Disease

Interventions

Sponsors

Maruyama Hideki
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Fasting LDL-C >= 70 mg/dL at randomization visit 2.Stable (greater than or equal to 4 weeks) and well-tolerated lipid-lowering regimen (including e.g. with or without Ezetimibe) that must include a high-intensity statin therapy with either atorvastatin greater than or equal to 40 mg QD or rosuvastatin greater than or equal to 20 mg QD 3.Established CV disease defined as ANY of the following three conditions -Spontaneous Myocardial infarction >= 4 weeks from screening visit -History of ischemic stroke occurred >= 4 weeks prior to the Screening visit -Symptomatic peripheral arterial disease (PAD) evidenced by either intermittent claudication with ankle brachial index (ABI) < 0.85, prior peripheral arterial revascularization procedure, or, amputation due to atherosclerotic disease.

Exclusion criteria

Exclusion criteria: 1.Acute coronary syndrome, stroke, peripheral arterial revascularization procedure or amputation due to atherosclerotic disease < 4 weeks before screening visit 2.Treatment with PCSK9 inhibitors (e.g. evolocumab, alirocumab) within 90 days or planned use post first study visit 3.Planned or expected cardiac, cerebrovascular or peripheral artery surgery or re-vascularization within the 6 months after the first study visit 4.Heart failure NYHA class III or IV 5.Active liver disease defined as any known current infectious, neoplastic, or metabolic pathology of the liver 6.Previous exposure to inclisiran or any other non-mAb PCSK9-targeted therapy, either as an investigational or marketed drug within 2 years 7.Severe concomitant non-CV disease that is expected to reduce life expectancy to less than 5 years 8.History of malignancy that required surgery radiation therapy and/or systemic therapy during the 3 years prior to the first study visit 9.Pregnant or nursing (lactating) women

Design outcomes

Primary

MeasureTime frame
Time to First Occurrence of 3P-MACE

Countries

Argentina, Australia, Austria, Belgium, Brazil, Bulgaria, Canada, Chile, China, Croatia, Czechia, Denmark, Estonia, Finland, France, Hungary, India, Israel, Italy, Japan, Korea, Republic of, Latvia, Lithuania, Malaysia, Mauritius, Mexico, Netherlands, New Zealand, Norway, Philippines, United States

Contacts

Public ContactHideki Maruyama

Novartis Pharma. K.K.

rinshoshiken.toroku@novartis.com+81-120-003-293

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026