Study of Evolocumab to Prevent Heart Disease Events in High-Risk Patients Without Previous Heart Attack or Stroke

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What is this study about?

This study focuses on people at high risk of cardiovascular disease who have not previously experienced a myocardial infarction (heart attack) or stroke. The research examines the effectiveness of a medication called evolocumab (also known as AMG 145) compared to placebo in preventing serious heart and blood vessel problems. Evolocumab is a medication that helps lower cholesterol levels in the blood.

The study aims to determine if evolocumab can reduce the risk of death from coronary heart disease, heart attacks, and strokes in people receiving standard cholesterol-lowering therapy. The medication is given as an injection under the skin using a pre-filled pen that contains 140 mg of evolocumab.

During the study, participants will receive either evolocumab injections or placebo injections. The treatment period lasts for 72 weeks, during which participants will continue their usual cholesterol-lowering medications. The study will track various heart-related health events, including arterial revascularization (procedures to restore blood flow in blocked arteries) and death from heart-related causes.

1 Initial treatment assignment

You will be randomly assigned to receive either evolocumab or a placebo (an inactive substance).

The assignment is double-blind, which means neither you nor your doctor will know which treatment you are receiving.

2 Treatment administration

You will receive subcutaneous injections (under the skin) of either evolocumab or placebo.

The treatment will continue throughout the study period, which runs until June 30, 2025.

3 Ongoing medical care

You will continue receiving your regular lipid-lowering therapy (medications to control cholesterol) throughout the study.

Regular monitoring of your heart health and blood tests will be conducted to track your progress.

4 Health monitoring

Your health will be monitored for important heart-related events, including:

– Heart problems (coronary heart disease)

– Heart attacks (myocardial infarction)

– Brain blood vessel blockages (ischemic stroke)

– Need for blood vessel procedures (arterial revascularization)

5 Study completion

The study will conclude on June 30, 2025.

Your participation will help determine if evolocumab reduces the risk of serious heart-related events in patients at high cardiovascular risk.

Who Can Join the Study?

  • Age requirements: men must be 50 years or older, women must be 55 years or older, and all participants must be under 80 years old
  • Must have specific blood fat levels:
    • LDL (bad cholesterol) of at least 90 mg/dL, or
    • non-HDL cholesterol of at least 120 mg/dL, or
    • apolipoprotein B of at least 80 mg/dL
  • Must have at least one of these heart-related conditions:
    • Significant heart artery disease with previous procedures or blockages
    • Significant blood vessel problems affecting the brain
    • Significant blood vessel problems in the legs
    • Diabetes with complications affecting small blood vessels
  • Must have at least one additional risk factor:
    • Blood vessel disease in multiple areas of the body
    • Diabetes or metabolic syndrome
    • Very high cholesterol levels
    • High levels of lipoprotein(a) in blood
    • Inherited high cholesterol
    • Family history of early heart disease
    • High levels of inflammation markers in blood
    • Current smoker
    • Over 65 years of age
    • Early menopause (before age 40)
    • Reduced kidney function
    • High calcium buildup in heart arteries

Who Cannot Join the Study?

  • Prior history of heart attack (myocardial infarction) or stroke
  • Currently participating in other clinical research studies
  • Known allergies to the study medication (evolocumab) or its components
  • Significant liver disease or abnormal liver function tests
  • Severe kidney problems (severe renal impairment)
  • Uncontrolled high blood pressure
  • History of serious bleeding disorders
  • Pregnant women or women planning to become pregnant during the study
  • Breastfeeding mothers
  • Active cancer or cancer treatment within the past 5 years
  • History of substance abuse within the past year
  • Mental conditions that could interfere with study participation
  • Unable to provide informed consent
  • History of not following medical treatment plans
  • Taking medications that could interact with the study drug

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
Clinique Pasteur Toulouse France
Medical University Of Vienna Vienna Austria
Sydvestjysk Sygehus Esbjerg Denmark
Medizinische Universitaet Innsbruck Innsbruck Austria
Oncopole Claudius Regaud Toulouse France
Technische Universitaet Dresden Dresden Germany
Katholieke Universiteit te Leuven Leuven Belgium
Hospital Universitario Y Politecnico La Fe Valencia Spain
Unidade Local De Saude De Lisboa Ocidental E.P.E. Carnaxide Portugal
Hospital Universitario De Navarra Pamplona Spain
CHU Grenoble Alpes La Tronche France
Falu lasarett Falun Sweden
Szpital św. Anny w Miechowie Miechow Poland
Frisius Heerenveen The Netherlands
Oblastní nemocnice Kladno, a.s. Kladno Czechia
Ctc Hodonín s.r.o. Hodonin Czechia
Oralek s.r.o. Namestovo Slovakia
Veselibas Centrs 4 SIA Riga Latvia
Gesundheitsverbund Landkreis Konstanz gGmbH Singen (Hohentwiel) Germany
Futuremeds Sp. z o.o. Wroclaw Poland
Kardiologie COR s.r.o. Prague Czechia
Zuyderland Medisch Centrum Stichting Geleen The Netherlands
Hopital Cardiologique Lille France
Stichting OLVG Amsterdam The Netherlands
Krakowskie Centrum Medyczne Sp. z o.o. Cracow Poland
Acibadem City Clinic Diagnostic And Consultation Center Tokuda EAD Sofia Bulgaria
Niepubliczny Zaklad Opieki Zdrowotnej Przychodnia Specjalistyczna A Wittek H Rudzki Sp. j. Ruda Slaska Poland
Nemocnice Pardubickeho kraje a.s. Pardubice Czechia
Algemeen Stedelijk Ziekenhuis Campus Aalst Aalst Belgium
Kardiologijos ir reabilitacijos klinika UAB Klaipeda Lithuania
MVZ im Altstadt-Carree Fulda GmbH Fulda Germany

Other Sites

Site Name City Country Status
Diagnostic & Therapeutic Center Of Athens Hygeia Single Member S.A. Athens Greece
Multiprofile Hospital For Active Treatment Knyaginya Klementina Sofia EAD Sofia Bulgaria
Ospedale San Raffaele S.r.l. Milan Italy
Semmelweis University Budapest Hungary
Sygehus Lillebaelt Vejle Sygehus Vejle Denmark
Spitalul Universitar De Urgenta Bucuresti Bucharest Romania
Centre Hospitalier Universitaire De Nantes Nantes France
Centre Hospitalier Universitaire De Nice Nice France
Hopital Beaujon Clichy France
Amphia Hospital Breda The Netherlands
Interna SK s.r.o. Svidnik Slovakia
Hospital Clinico Universitario De Valladolid Valladolid Spain
Otto Von Guericke Universitaet Magdeburg Magdeburg Germany
Pratia Prague s.r.o. Prague Czechia
Central Hospital Of Northern Pest Military Hospital Budapest Hungary
Centre Hospitalier De Versailles Le Chesnay-Rocquencourt France
Centre Hospitalier Sud Francilien Corbeil Essonnes France
Clinexpert Kft. Budapest Hungary
Medicus Services s.r.o. Brandys Nad Labem Czechia
Areteus s.r.o. Trebisov Slovakia
Marek Piepiorka GABINET KARDIOLOGICZNO – INTERNISTYCZNY Gdynia Poland
Sal Med S.R.L. Pitesti Romania
Nemocnice Pardubickeho kraje, Svitavska nemocnice a.s Svitavy Czechia
Sanos A/S Gandrup Denmark
Diabet2 s.r.o. Prague Czechia
Clinical Trials Service s.r.o. Uherske Hradiste Czechia
Center for Clinical and Basic Research AS Tallin Estonia
Assistance Publique Hopitaux De Paris Paris France
St. Antonius Ziekenhuis Nieuwegein The Netherlands
Uniteversity Muliprofile Hospital For Active Treatment Tsaritsa Yoanna-Isul EAD Sofia Bulgaria
Markhot Ferenc Oktatokorhaz Es Rendelointezet Eger Hungary
Centrum Badan Klinicznych Piotr Napora Lekarze sp.p. Wroclaw Poland
Multidisciplinary Hospital For Active Treatment Haskovo AD Haskovo Bulgaria
Klinik Hietzing Vienna Austria
Reinier de Graaf Groep Delft The Netherlands
Vojenska Nemocnice Brno Brno-Zidenice Czechia
Niepubliczny Zaklad Opieki Zdrowotnej Twoja Przychodnia Sp. z o.o. Lublin Poland
KliFoCenter GmbH Witten Germany
Amkardia s.r.o. Brno-Stred Czechia
CHU Helora La Louviere Belgium
Canisius Wilhelmina Ziekenhuis Nijmegen The Netherlands
Instytut Centrum Zdrowia Matki Polki Lodz Poland
Bekes Varmegyei Koezponti Korhaz Gyula Hungary
Zentrum Fur Klinische Studien Dr. Hanusch GmbH Vienna Austria
Medif Thuin Belgium
Copernicus Podmiot Leczniczy Sp. z o.o. Gdansk Poland
Unidade Local De Saude Do Alto Ave E.P.E. Guimaraes Portugal
BKS Research Kft. Hatvan Hungary
Bernhoven B.V. Uden The Netherlands
Stift Carlanderska Sjukhuset Gothenburg Sweden
Rode Kruis Ziekenhuis B.V. Beverwijk The Netherlands
Clinique Saint Hilaire Rouen France
Pedicor Trial s.r.o. Ostrava Czechia
Prywatne Centrum Kardiologii Torun Poland
Dika centrum s.r.o. Havirov Czechia
Cgcntqwvd Unecvhvrtmitex Sskvdhwrb Woluwe-Saint-Lambert Belgium
Uvyiegjyxj Mfzceeewuhmb Hakajmjw Fgx Azjsrj Tyukmfkrp Akl Envgtnlrn Megxxodj N I Pekblop Sofia Bulgaria
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Kughne Cvacuy Kmkvrqhpj Sgk z ouox Lublin Poland
Kplkfhotkqcxn Nuogo sfdrsl Nitra Slovakia
Jmiomldxobvfrvpnaojd Vxfrsgguj Hzgkvrx Gjwk Khbccxdzswfywfczvriei Szolnok Hungary
Koacttms Sldah Jxuvv Kyxxtj Komarom Hungary
Uaytx Msi Gnoibkx Gdsqok Hbps Mxkjiynhdw Dh Gwdvweia Grenoble France
Nzjjwpgiy Axwf Teixrbjmrwodkk ajen Konska Czechia
Hazosjinabplrwntnypuhfxssxync Mfs Ad Ffmvdmrwnofn Gxqs Dresden Germany
Cxobejpp Btsx Sdybtsxdo Sot z ohmb Sdge Lublin Poland
Ssuswdybfzt Pbbesgejn Sfwftjnhpeamahu Sevwgqq Znmwzbvh Iakgriteum Pdius It Grodzisk Mazowiecki Poland
Apual sxxztz Bardejov Slovakia
Pcjlcv Bmqq sluwjc Brno-Stred Czechia
Aastou Ssiagwrvvp Zonpsqpptd Dordrecht The Netherlands
Zlkcjfuigv Rjmdvwzudqmz Tiel The Netherlands
Sjjgzrlki Hhenzjzgvutstagr Gadqtddhbpnwvguqlu Skovde Sweden
Cxroba Mzw Szevem Craiova Romania
Mdnczx Sdwzue Targu Mures Romania
Dwxffgtlpk rudkwgqvn syizaplb Szo Daugavpils Latvia
Synjxthxu Vxxwdul Msdohzv Cfrphbd vxzk Nujrmubnfguwg Venlo The Netherlands
Miifioqv snyfmy Bratislava Slovakia
Cew Obrhmlb snaidm Moravska Ostrava A Privoz Czechia
Lvz Hvcpkzuf Dd Cdazcqyg Le Coudray France
Kgbmymysikr scjfca Louny Czechia
Sxzcxgy Gtqfghoshf Iladw Mqne Ruqeph Mtwcvgbk Scy z oaim Warsaw Poland
Ef Hfteikvm Urwiymixdulxx Dq Guis Crjsten Dpk Nxqdyy Las Palmas De Gran Canaria Spain
Dpiardwtydreubm Seezxlfyz Utrecht The Netherlands
D &bqrl A Riwmfpjk Bbyp Sneek The Netherlands
Cyhuoqwr Rezrfyzz Cpromd Syl z opnq Mynxyvt sljct Poznan Poland
Zzogamkpocuovfd Tmvuhb Sgemkixby Almelo The Netherlands
Ezdfmkcfo Zwyithetpw Helmond The Netherlands
Wucpwskznp Srkfrvy Zegyampbr Itbjxgprkeuadx W Tqwaeac Torun Poland
Ciewrvoshxjqu Hupmbxk Gtu Hamburg Germany
Br Bagsh Akiyqnunss Huzwbyyalgk Khirqs Meh Gxka Kassel Germany
Zywbwcgrlx Sv Jcphbok Harderwijk The Netherlands
Ufyfwne Lreom Dc Suxaq Dg Myitstqcmm Eifexf Senhora Da Hora Portugal
Eedtouiu Gernwukmft Kdii Godollo Hungary
Kocrurp Mnrqrbh Ccergh Lrvq Sofia Bulgaria
Мltlxeughslzbvmzq hjfiehpq foq aixhxq tcfxaqkpx Sskqp Gwnjds Pojypu Ozp Pernik Bulgaria
Nyujdquo Mdnabhjkfiwfklimg Tkeoraahq Hkiepbae Tfzs Bcsus Iod Sofia Bulgaria
Iuzjxq Zpcfyqcdwt Rotterdam The Netherlands
Ozlpdipuv vob Tlptoj Dendermonde Belgium
Svirpyrv Om Jyvaskyla Finland
Mmkutqcbmhabw Hjnmlatj fsm Apaicy Tzwayaqng Hkbmw arn Bcguc Esu Pleven Bulgaria
Cpfqch Dqnvibf sbifjo Kcgyfy Kosice Slovakia
Pfrvobsxhj Kovo Bekescsaba Hungary
Drvv scvnol Roznava Slovakia
Pvgbvy 4 Tsmzb Ktup Gyongyos Hungary
Mesf Mvtqwwy swcfrb Moldava Nad Bodvou Slovakia
Hst Vry Wjzhdspahbolf Zropawgqsd Dirksland The Netherlands
Pjyvnsccxc Ai Malmo Sweden
Gxpvqur Hqzkcavs Og Nod Iwnqp Knmenadocwmwtski Pcewzyje Nea Ionia Greece
Vjcad scijtx Petrzalka Slovakia
Hehykjfa Urdsmpzjflwex Hqcybmgl Tjjjb y Pzlsyj Ihscbdsw Cxibvu doqiveajrzhtwczjw (mlie Badalona Spain
Srlsek Trzdjwffout Ol Turku Finland
Chbqwgdjt Ssh z ozoz Lublin Poland
Ombyzqmj nmjdwrohb Kvkxk ampb nfeadcdmj Syqndbubbacrl kgtbg Kolin Czechia
Iygxzqy a kiferwmslrscs otosainq Prague Czechia
Snfnjyvpnmd Pudfqzsnq Zjrngn Oxcyzk Zruayuckks W Ldrjwso Leczna Poland
Hzdftxxwwcmwnsgz exkl Kopavogur Iceland
Dfqkjfg vyv Nyztjxdsls Zwijndrecht The Netherlands
Hcakiqteslllcixflm Revcbkyxrs Bvjh Hague The Netherlands
Eyi Mfdilxvbxpgtbnif Srtrrrmljhnmmxl Prrluqvl Lokdqmea Cracow Poland
Kjjsgl 1 sgpupo Lučenec Slovakia
Urgkana Ddgfvoggbtx kkem Teplice Czechia
Mlgzxpkvb Cwbhenc Zfmlguj Sqwi Lublin Poland
Naawakzpontb Zbfahg Obnejc Zztzvtrjzz Mkleiz Jnzvx Cqrwlo Giżycko Poland
Tbnemf Bnmmknlnmn Lgbaacndh Cinomdq Dlafvqdwcjfyj Swidnik Poland
Mproldtwtcht Hdgnvyvl Fwc Airtwa Tukjnaszk Mhcfknj Cobsejx Syopy Ikqc Rkiokx Erzp Plovdiv Bulgaria

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Austria Austria
Not recruiting
18.06.2019
Belgium Belgium
Not recruiting
18.06.2019
Bulgaria Bulgaria
Not recruiting
18.06.2019
Czechia Czechia
Not recruiting
18.06.2019
Denmark Denmark
Not recruiting
18.06.2019
Estonia Estonia
Not recruiting
18.06.2019
Finland Finland
Not recruiting
18.06.2019
France France
Not recruiting
18.06.2019
Germany Germany
Not recruiting
18.06.2019
Greece Greece
Not recruiting
18.06.2019
Hungary Hungary
Not recruiting
18.06.2019
Iceland Iceland
Not recruiting
18.06.2019
Italy Italy
Not recruiting
18.06.2019
Latvia Latvia
Not recruiting
18.06.2019
Lithuania Lithuania
Not recruiting
18.06.2019
Poland Poland
Not recruiting
18.06.2019
Portugal Portugal
Not recruiting
18.06.2019
Romania Romania
Not recruiting
18.06.2019
Slovakia Slovakia
Not recruiting
18.06.2019
Spain Spain
Not recruiting
18.06.2019
Sweden Sweden
Not recruiting
18.06.2019
The Netherlands The Netherlands
Not recruiting
18.06.2019

Trial locations

Investigated Drugs:

Evolocumab is a medication that helps lower cholesterol levels in the blood. It works by blocking a protein that prevents the liver from removing LDL (bad) cholesterol from the blood. This medication is used in patients who have a high risk of cardiovascular problems but haven’t had a heart attack or stroke. It is given alongside other cholesterol-lowering treatments to help reduce the risk of serious heart problems.

Placebo is an inactive substance that looks identical to the real medication but contains no active ingredients. It is used to help determine if the actual medication is effective.

Note: Both medications in this trial are given to patients who are already receiving optimized lipid-lowering therapy as part of their standard treatment for managing cardiovascular risk.

Coronary Heart Disease (CHD) – A condition where the main blood vessels that supply the heart become narrowed or blocked by fatty deposits. This process develops gradually over time as cholesterol and other materials build up on the inner walls of arteries. The reduced blood flow can cause chest pain and eventually lead to a heart attack if a coronary artery becomes completely blocked. The disease often progresses silently for many years before showing symptoms.

Myocardial Infarction (MI) – A condition where part of the heart muscle is damaged due to insufficient blood supply. It occurs when one or more coronary arteries become blocked, preventing oxygen-rich blood from reaching certain areas of the heart. The affected heart muscle begins to die within minutes of being deprived of oxygen. The damage can vary in size and severity depending on the duration and location of the blockage.

Ischemic Stroke – A condition where blood flow to a part of the brain is blocked, typically by a blood clot. When brain tissue is deprived of oxygen and nutrients, brain cells begin to die within minutes. The effects of an ischemic stroke depend on which area of the brain is affected and how much tissue is damaged. The condition can cause sudden weakness, confusion, or difficulty speaking.

Cardiovascular Disease – A group of disorders affecting the heart and blood vessels throughout the body. The condition typically develops when arteries become hardened and narrowed due to the buildup of fatty deposits. This process can affect blood vessels throughout the body, including those supplying the heart, brain, and other vital organs. The disease often develops gradually over many years.

Trial ID:
2023-503673-38-00
Protocol code:
20170625
NCT ID:
NCT03872401
Trial Phase:
Therapeutic confirmatory (Phase III)

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