Evolocumab
DrugAdministered subcutaneously using an autoinjector pen.
Other names: AMG 145, Repatha
NCT Number: NCT03872401
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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Notify Me50 year–79 year
All sexes
Interventional
Phase 3
Instituto de Investigaciones Clinicas Bahia Blanca, Bahía Blanca, Buenos Aires, Argentina
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
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:
B. Significant atherosclerotic cerebrovascular disease meeting at least 1 of the following criteria:
C. Significant peripheral arterial disease meeting at least 1 of the following criteria:
D. Diabetes mellitus with at least 1 of the following:
•At least 1 of the following 1 high-risk criteria (most recent lab values within 6 months prior to screening, as applicable):
-≥65 years of age.
Exclusion criteria
Administered subcutaneously using an autoinjector pen.
Other names: AMG 145, Repatha
Administered subcutaneously using an autoinjector pen.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Amgen
Industry
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
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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