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OpenTrials
Completed

NCT Number: NCT03872401

Effect of Evolocumab in Patients at High Cardiovascular Risk Without Prior Myocardial Infarction or Stroke

This study will assess the effect of lowering low-density lipoprotein cholesterol (LDL-C) with evolocumab on major cardiovascular events in adults without a prior myocardial infarction (MI) or stroke who are at high risk of a cardiovascular event.

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Key information

Age range

50 year–79 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Instituto de Investigaciones Clinicas Bahia Blanca, Bahía Blanca, Buenos Aires, Argentina

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age: Adult participants ≥ 50 (men) or ≥ 55 (women) to ˂ 80 years of age (either sex) and meeting lipid criteria.
  • Lipid Criteria: Low-density lipoprotein cholesterol (LDL-C) ≥ 90 mg/dL (≥ 2.3 mmol/L) or non high-density lipoprotein cholesterol (non-HDL)-C ≥ 120 mg/dL (≥ 3.1 mmol/L), or apolipoprotein B ≥ 80 mg/dL (≥ 1.56 µmol/L).

3.Diagnostic evidence of at least one of the following (A-D) at screening:

A.Significant coronary artery disease (CAD) meeting at least 1 of the following criteria:

  • History of coronary revascularization with multi-vessel coronary disease as evidenced by any of the following:
  • percutaneous coronary intervention (PCI) of 2 or more vessels, including branch arteries,
  • PCI or coronary artery bypass grafting (CABG) with residual 50% stenosis in a separate, unrevascularized vessel, or
  • multi-vessel CABG 5 years or more prior to screening.
  • Significant coronary disease without prior revascularization as evidenced by either a ≥70% stenosis of at least 1 coronary artery, ≥50% stenosis of 2 or more coronary arteries, or ≥50% stenosis of the left main coronary artery.
  • known coronary artery calcium score ≥100 in participants without a coronary artery revascularization prior to randomization.

B. Significant atherosclerotic cerebrovascular disease meeting at least 1 of the following criteria:

  • prior transient ischemic attack with ≥50% carotid stenosis.
  • internal or external carotid artery stenosis of ≥70% or 2 or more ≥50% stenoses.
  • prior internal or external carotid artery revascularization.

C. Significant peripheral arterial disease meeting at least 1 of the following criteria:

  • ≥50% stenosis in a limb artery.
  • history of abdominal aorta treatment (percutaneous and surgical) due to atherosclerotic disease.
  • ankle brachial index (ABI) <0.85.

D. Diabetes mellitus with at least 1 of the following:

  • known microvascular disease, defined by diabetic nephropathy or treated retinopathy. Diabetic nephropathy defined as persistent microalbuminuria (urinary albumin to creatinine ratio ≥30mg/g) and/or persistent estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m^2 that is not reversible due to an acute illness.
  • chronic daily treatment with an intermediate or long-acting insulin.
  • diabetes diagnosis ≥10 years ago.

•At least 1 of the following 1 high-risk criteria (most recent lab values within 6 months prior to screening, as applicable):

  • Polyvascular disease, defined as coronary, carotid, or peripheral artery stenosis ≥50% in a second distinct vascular location in a participant with coronary, cerebral or peripheral arterial disease (A, B, or C above).
  • Presence of either diabetes mellitus or metabolic syndrome in a participant with coronary, cerebral, or peripheral artery disease (A, B, or C above).
  • At least 1 coronary, carotid, or peripheral artery residual stenosis of ≥50% in a participant with diabetes meeting inclusion criterion (D above).
  • LDL-C ≥130 mg/dL (≥3.36 mmol/L), OR non-HDL-C ≥160 mg/dL (≥4.14 mmol/L), OR apolipoprotein B ≥120 mg/dL (2.3 µmol/L) if available.
  • Lipoprotein (a) >125 nmol/L (50 mg/dL).
  • Known familial hypercholesterolemia.
  • Family history of premature coronary artery disease defined as an MI or CABG in the participant's father or brother at age <55 years or an MI or CABG in the participant's mother or sister at age <60 years.
  • High sensitive c-reactive protein (hsCRP) ≥3.0 mg/L in the absence of an acute illness.
  • Current tobacco use.

-≥65 years of age.

  • Menopause before 40 years of age.
  • eGFR 15 to <45 mL/min/1.73 m^2.
  • Coronary artery calcification score ≥300 in a participant without a coronary revascularization prior to randomization.

Exclusion criteria

  • MI or stroke prior to randomization.
  • CABG ˂ 3 months prior to screening.
  • eGFR ˂ 15 mL/min/1.73 m^2.
  • Uncontrolled or recurrent ventricular tachycardia in the absence of an implantable-cardioverter defibrillator.
  • Atrial fibrillation or atrial flutter not on anticoagulation therapy (vitamin K antagonist, heparin, low molecular weight heparin, fondaparinux,or non-Vitamin K antagonist oral anticoagulant).
  • Triglycerides ≥ 500 mg/dL (5.7 mmol/L) measured up to 3 months prior to screening. The most recent results must be used.
  • Last measured left-ventricular ejection fraction ˂ 30% or New York Heart Association (NYHA) Functional Class III/IV.
  • Planned arterial revascularization.

Treatment and study plan

Evolocumab

Drug

Administered subcutaneously using an autoinjector pen.

Other names: AMG 145, Repatha

Placebo

Drug

Administered subcutaneously using an autoinjector pen.

Primary outcomes

  1. Number of Participants Who Experienced Coronary Heart Disease (CHD) Death, Myocardial Infarction (MI), or Ischemic Stroke, Whichever Occurred First

    Time frame: From enrollment to last confirmed survival status date; median (min, max) time on trial was 55.2 (0.0, 72.7) months

    All deaths and individual components were adjudicated by an independent external clinical events committee (CEC), using standardized definitions. The number of participants who experienced CHD death, MI, or ischemic stroke, whichever occurred first, among participants at high cardiovascular risk without prior MI or stroke and were receiving optimized lipid lowering therapy was analyzed.

  2. Number of Participants Who Experienced CHD Death, MI, Ischemic Stroke, or Any Ischemia-driven Arterial Revascularization, Whichever Occurred First

    Time frame: From enrollment to last confirmed survival status date; median (min, max) time on trial was 55.2 (0.0, 72.7) months

    All deaths and individual components were adjudicated by an independent external CEC, using standardized definitions. The number of participants who experienced CHD death, MI, ischemic stroke, or any ischemia-driven arterial revascularization, whichever occurred first, among participants at high cardiovascular risk without prior MI or stroke and were receiving optimized lipid lowering therapy was analyzed.

Secondary outcomes

  1. Number of Participants Who Experienced MI, Ischemic Stroke, or Any Ischemia-driven Arterial Revascularization

    Time frame: From enrollment to last confirmed survival status date; median (min, max) time on trial was 55.2 (0.0, 72.7) months

    All deaths and individual components were adjudicated by an independent external CEC, using standardized definitions. The number of participants who experienced MI, ischemic stroke, or any ischemia-driven arterial revascularization, among participants at high cardiovascular risk without prior MI or stroke and were receiving optimized lipid lowering therapy was analyzed.

  2. Number of Participants Who Experienced CHD Death, MI, or Any Ischemia-driven Arterial Revascularization

    Time frame: From enrollment to last confirmed survival status date; median (min, max) time on trial was 55.2 (0.0, 72.7) months

    All deaths and individual components were adjudicated by an independent external CEC, using standardized definitions. The number of participants who experienced CHD death, MI, or any ischemia-driven arterial revascularization, among participants at high cardiovascular risk without prior MI or stroke and were receiving optimized lipid lowering therapy was analyzed.

  3. Number of Participants Who Experienced Cardiovascular Death, MI, or Ischemic Stroke

    Time frame: From enrollment to last confirmed survival status date; median (min, max) time on trial was 55.2 (0.0, 72.7) months

    All deaths and individual components were adjudicated by an independent external CEC, using standardized definitions. The number of participants who experienced cardiovascular death, MI, or ischemic stroke, among participants at high cardiovascular risk without prior MI or stroke and were receiving optimized lipid lowering therapy was analyzed.

  4. Number of Participants Who Experienced CHD Death or MI

    Time frame: From enrollment to last confirmed survival status date; median (min, max) time on trial was 55.2 (0.0, 72.7) months

    All deaths and individual components were adjudicated by an independent external CEC, using standardized definitions. The number of participants who experienced CHD death or MI, among participants at high cardiovascular risk without prior MI or stroke and were receiving optimized lipid lowering therapy was analyzed.

  5. Number of Participants Who Experienced MI

    Time frame: From enrollment to last confirmed survival status date; median (min, max) time on trial was 55.2 (0.0, 72.7) months

    All deaths and individual components were adjudicated by an independent external CEC, using standardized definitions. The number of participants who experienced MI, among participants at high cardiovascular risk without prior MI or stroke and were receiving optimized lipid lowering therapy was analyzed.

  6. Number of Participants Who Experienced Any Ischemia-driven Arterial Revascularization

    Time frame: From enrollment to last confirmed survival status date; median (min, max) time on trial was 55.2 (0.0, 72.7) months

    All deaths and individual components were adjudicated by an independent external CEC, using standardized definitions. The number of participants who experienced ischemia-driven arterial revascularization, among participants at high cardiovascular risk without prior MI or stroke and were receiving optimized lipid lowering therapy was analyzed.

  7. Number of Participants Who Experienced CHD Death

    Time frame: From enrollment to last confirmed survival status date; median (min, max) time on trial was 55.2 (0.0, 72.7) months

    All deaths and individual components were adjudicated by an independent external CEC, using standardized definitions. The number of participants who experienced CHD death, among participants at high cardiovascular risk without prior MI or stroke and were receiving optimized lipid lowering therapy was analyzed.

  8. Number of Participants Who Experienced Cardiovascular Death

    Time frame: From enrollment to last confirmed survival status date; median (min, max) time on trial was 55.2 (0.0, 72.7) months

    All deaths and individual components were adjudicated by an independent external CEC, using standardized definitions. The number of participants who experienced cardiovascular death, among participants at high cardiovascular risk without prior MI or stroke and were receiving optimized lipid lowering therapy was analyzed.

  9. Number of Participants Who Died Due to Any Cause

    Time frame: From enrollment to last confirmed survival status date; median (min, max) time on trial was 55.2 (0.0, 72.7) months

    All deaths and individual components were adjudicated by an independent external CEC, using standardized definitions. The number of participants who died due to any cause, among participants at high cardiovascular risk without prior MI or stroke and were receiving optimized lipid lowering therapy was analyzed.

  10. Number of Participants Who Experienced Ischemic Stroke

    Time frame: From enrollment to last confirmed survival status date; median (min, max) time on trial was 55.2 (0.0, 72.7) months

    All deaths and individual components were adjudicated by an independent external CEC, using standardized definitions. The number of participants who experienced ischemic stroke, among participants at high cardiovascular risk without prior MI or stroke and were receiving optimized lipid lowering therapy was analyzed.

Sponsors and collaborators

Lead sponsor

Amgen

Industry

Registry information

Official study title

A Double-blind, Randomized, Placebo-controlled, Multicenter Study to Evaluate the Impact of Evolocumab on Major Cardiovascular Events in Patients at High Cardiovascular Risk Without Prior Myocardial Infarction or Stroke

Acronym: VESALIUS-CV

Important dates

Study start
2019
Primary completion
2025
Study completion
2025
First posted
Mar 13, 2019
Registry last updated
Jun 25, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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