A study to evaluate the effect of muvalaplin on reducing major cardiovascular events in adults with high levels of lipoprotein(a) and atherosclerotic cardiovascular disease.

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What is this study about?

This study focuses on individuals with high levels of Lipoprotein(a), which is a type of fatty particle in the blood that can increase the risk of heart issues. The research also involves people living with Atherosclerotic Cardiovascular Disease, a condition where plaque builds up in the arteries, potentially leading to serious health problems. The purpose of this study is to evaluate whether the drug muvalaplin can help reduce the occurrence of Major Adverse Cardiovascular Events, which are serious heart-related problems such as heart attacks or strokes.

Participants in the study will be assigned to receive either muvalaplin, which is taken as an oral tablet, or a placebo. This is a randomized study, meaning the treatment assigned is determined by chance, and it is double-blind, so neither the participants nor the researchers know which treatment is being given during the trial. The study will monitor how the medication affects the risk of experiencing major heart events over time.

Who Can Join the Study?

  • You must have high levels of Lp(a), which is a specific type of protein in your blood that can contribute to heart problems, with a level of 175 nmol/L or more.
  • You must have experienced a previous heart-related event, such as a heart attack (when blood flow to the heart is blocked), a stroke (when blood flow to the brain is blocked), or have had a procedure to improve blood flow to your heart or other parts of your body.
  • Alternatively, you may qualify if you are at risk for your first heart event and have coronary artery disease (narrowing of the arteries that supply blood to the heart), carotid stenosis (narrowing of the arteries in the neck that lead to the brain), or peripheral artery disease (narrowing of the blood vessels that carry blood to the legs or arms).
  • You may also qualify if you have a high coronary artery calcium score, which is a measurement used to check for calcium buildup in the arteries of the heart.
  • You may also qualify if you have reduced kidney function (your kidneys are not filtering blood as well as they should) and also have diabetes.
  • You may also qualify if you have a combination of other high-risk factors that increase the chance of heart problems.

Who Cannot Join the Study?

  • You cannot participate if you have had a major heart or blood vessel event, which is a serious medical emergency involving the heart or the tubes that carry blood, within 90 days before starting the study.
  • You cannot participate if you are planning to have any surgery on your heart or your arteries, which are the blood vessels that carry oxygen-rich blood away from the heart.
  • You cannot participate if you have very high blood pressure or serious heart failure, a condition where the heart cannot pump blood effectively enough to meet the body’s needs.
  • You cannot participate if you have had or are planning to have a procedure to remove cholesterol from the blood within 90 days before starting the study.
  • You cannot participate if you have severe kidney failure, which means your kidneys are not working well enough to filter waste from your blood.
  • You cannot participate if you have a history of cancer, meaning you have been diagnosed with or treated for cancer, within 5 years before starting the study.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
Linden Sp. z o.o. sp.k. Cracow Poland
Medical University Of Vienna Vienna Austria
NOE Landesgesundheitsagentur Mistelbach Austria
University Medicine Greifswald Greifswald Germany
Klinische Forschung Karlsruhe GmbH Karlsruhe Germany
Ctc Hodonín s.r.o. Hodonin Czechia
Gyncentrum Sp. z o.o. Katowice Poland
Centre Hospitalier Universitaire De Lille Lille France
Futuremeds Sp. z o.o. Wroclaw Poland
Azienda Ospedaliero Universitaria Careggi Florence Italy
Oncopole Claudius Regaud Toulouse France
Technische Universitaet Dresden Dresden Germany
Katholieke Universiteit te Leuven Leuven Belgium
Bellvitge University Hospital L'hospitalet De Llobregat Spain
Stichting OLVG Amsterdam The Netherlands
Premedix Bratislava Slovakia
Imed19-Privat Vienna Austria
Kormont Kluisbergen Belgium
CHU Grenoble Alpes La Tronche France
Institutul National de Diabet, Nutritie si Boli Metabolice “N.C. Paulescu” Bucharest Romania
Cardio Metabolic Centre Mattersburg Austria

Other Sites

Site Name City Country Status
Central Hospital Of Northern Pest Military Hospital Budapest Hungary
Coromed-Smo Kft. Pecs Hungary
MVZ CCB Frankfurt Und Main-Taunus GbR Frankfurt Germany
Evangelisches Krankenhaus Witten gGmbH Witten Germany
Sanos A/S Gandrup Denmark
Diabet2 s.r.o. Prague Czechia
Vranovska nemocnica a.s. Vranov Nad Toplou Slovakia
Assistance Publique Hopitaux De Paris Paris France
Ospedale San Raffaele S.r.l. Milan Italy
Fakultni Nemocnice Hradec Kralove Novy Hradec Kralove Czechia
Az St-Jan Brugge-Oostende A.V. Brugge Belgium
Semmelweis University Budapest Hungary
Hospital Universitario De Leon Leon Spain
Centre Hospitalier Saint Joseph Saint Luc Lyon France
Spitalul Universitar De Urgenta Bucuresti Bucharest Romania
Hospital General Universitario De Valencia Valencia Spain
Klinik Hietzing Vienna Austria
Centre Hospitalier Universitaire De Nantes Nantes France
Centre Hospitalier Universitaire De Nice Nice France
Wilhelmina Ziekenhuis Assen Assen The Netherlands
Azienda Ospedaliero Universitaria Di Modena Modena Italy
Hopital Beaujon Clichy France
Hospital Del Mar Barcelona Spain
Canisius Wilhelmina Ziekenhuis Nijmegen The Netherlands
Instytut Centrum Zdrowia Matki Polki Lodz Poland
Nutrilife S.R.L. Bucharest Romania
Klinische Forschung Berlin-Mitte GmbH Berlin Germany
Zentrum Fur Klinische Studien Dr. Hanusch GmbH Vienna Austria
Gensan S.R.L. Sibiu Romania
MVZ Rheumatologie und Autoimmunmedizin Hamburg GmbH Hamburg Germany
Gottsegen National Cardiovascular Center Budapest Hungary
A.O. Krankenhaus St. Josef Braunau GmbH Braunau Am Inn Austria
Irmed Klimkiewicz Rudziewicz-Kowalska sp. j. Piotrkow Trybunalski Poland
Hospital Virgen De Las Montanas Villamartin Spain
General Hospital Of Thessloniki G Gennimatas Thessaloniki Greece
EB FlevoResearch B.V. Almere The Netherlands
St. Josefskrankenhaus Heidelberg GmbH Heidelberg Germany
MUDr. Simon Jirat s.r.o. Prague Czechia
Hospital Civil de Málaga Malaga Spain
Otto Von Guericke Universitaet Magdeburg Magdeburg Germany
Azorg Aalst Belgium
Klinische Forschung Schwerin GmbH Schwerin Germany
Association Hospitaliere De Bruxelles Et De Schaerbeek Centre Hospitalier Universitaire Brugmann Brussels Belgium
4 Wojskowy Szpital Kliniczny z Polikliniką SPZOZ Wroclaw Poland
Praxis Oedeme Lueneburg Germany
Zixkoplqzn Gggwarmb Vrenso Sfdasijzw Ede The Netherlands
Cgqyaxuzu Uuxmkskbnvhkyg Sedctuesl Woluwe-Saint-Lambert Belgium
Axeiynp Oamhonvqjxx dn Pkslyu Padua Italy
Hqldwxrt Msdanoo Snqxpgyo Stgocy Bucharest Romania
Hctubcq Sgizp Auxrgpq Paris France
Egchlczxakxs Sqqy Athens Greece
Msbelvyl Mechelen Belgium
Ngg Lfv Gpsvpgfxad Rnuikc Mfyox Gtru St. Poelten Austria
Uyxtrftafg Grploxc Hcpzjphr Oz Tdkoovrmwkgx Auyoi Thessaloniki Greece
Nmkooth usqci sueavrcza a cwcnhjjh cxeuwb aleq Bratislava Slovakia
Cgu Dtw Pkzphxnow Cllybuax Targu Mures Romania
Uahqlaakal Gcxqtln Hdgisses Ot Iqoyyjfu Ioannina Greece
Hxtiqsgqym Utj Mvm Gewg Ulm Germany
Dmwfxbcvzriioq Srqlzj Targu Mures Romania
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Clbovt Hkbtkbhqnik Usvifmqykttdo Dd Pxblmjfk Poitiers France
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Lavjw Ujaxzoyccqdz Mdwgdqm Cronqvr (kiqhc Leiden The Netherlands
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Cwzgcrk Mnsjrfq Ucbcuf Siuywc Brasov Romania
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Riqyrp Ilrkukaq fhqi myaefwgqsmxp Siopprc uiv Fnzbxlkgpua Gwqn Oldenburg In Holstein Germany
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Meegxd Stwxp Sxbiae Galati Romania
Hieuabih Umvqvpwdriezp Irodiou Lubeln Madrid Spain
Hzbutemcyqeerxgrhsulhmxoshzdt Mfp An Fyaozngalwip Gifg Dresden Germany
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Kjcpbguto Ftwvbhrey Hihhvov Giqh Hamburg Germany
Arhrpl Svlgzxvsjz Zntcmnjqhj Dordrecht The Netherlands
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Chyquy Mkhcsqzv Mgdtjhbbt Sey z ormh Lodz Poland
Hqmfupwt Uewnvrkbxqved Vjfbks Da Lvf Nlyajd Granada Spain
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Vcnmf Feldkirch Austria
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Ppuxrksmdk Namur Belgium
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Exvauflpb Iuyczviov Fhd Ckzbwwbsupkmam Djnexlzk Abx Tcpchrwkur Targu Mures Romania
Nsafkviqn s ptbzmsnvkezj Smruyin Nayv Vhx asbt Spisska Nova Ves Slovakia
Dfteyjw smmkfr Bratislava Slovakia
Phbalrn Twjnf &cgos Rfhqbujxxlm Bqks Beek Lb The Netherlands
Nuqitytbq S Pxhdejighsao Sm Lchehi Gewffhg axlt Galanta Slovakia
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Pddur Hzigjnlzf Sy axgu Rimavska Sobota Slovakia
Dyeuaj Mdj Sezlsu Bucharest Romania
Mfcluli slkxms Malacky Slovakia
Sgctoebs Cwzhkt Dn Uayovhk Pkoe Dx Afqpizu Iqfmbsj Balotesti Romania
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Ukp Kbhewgtxj Fvfkogesp Essen Germany
Zroxokk fvu kegqbaybh Sflnpzy Bgx Hkhxwkd Bad Homburg Germany
imsp Srr Poqorqb Gybwpidtapxtu fjoq Igswia Mepvmjy Dgs Ahlcablhm Dok Bixxex Dct Kipti udy Dba Scuqfh Ov St. Poelten Austria
Nxcqfewje S Pmudjormfwow Ddrqwgez Soemen azgy Dunajská Streda Slovakia
Dhy Hcpwb stgkbs Latran Czechia
Isdqjxvv kbmvoly shylga Chrudim Czechia
Mdgzd Bxotkz sbaipg Ostrava Czechia
Cdusc lfxvpshmt srfsle Vresina Czechia
Evgdpujsmia Cqbuqzhbdronupqcmrxijclexb Budapest Hungary
Pitujgdjxyi Gjslxtsjl Spl z oixu Grudziadz Poland
Cjmvsvkc Hojsupwausxx Rgjmo Jwth Bjcmu Madrid Spain
Cqruypl Mvglmgmz &ibwiqkyolwcpmexlwvghvsp suai Edgwmstw i Gwjpmqxr Gelxhc Bydgoszcz Poland
Csdcwhhq swdfcq Prague Czechia
Aitmkuf Obukprukbnu Uaweuzmwwsvwo Skezkd Ferrara Italy
Cpxiutwf sqyrhv Prague Czechia
Hjisqfpf Ufvwqmtfqbvfq Vhyzcz Dt Lx Vifdkmvf Malaga Spain
Hsneowhq Itdbpbb Ejqns Huelva Spain
Klclhjn Dil Boxdoxdxnnqt Bcfujpn Linz Austria
Pkcofl fna Itmfos Mceulsbh Kdehirwziezh Agdyqczunix Psawquszfnk uaz Aqzckbzbbomy Mannheim Germany
Hndeluup Uwuaqwolmgtmcl Suhxlndjyu &cccpdm Hlrxguh ds Hgiundbedsd STRASBOURG, Alsace France
Uzwtvowbudt Skkedloc Salzburg Austria
Bcdkhijn Ddspibnh Rigkkcbi Cbfxuo Bxpa Hoogeveen The Netherlands
Asrdo Tjnea Rulrjcno Kzyn Oroshaza Hungary
Mjpbkj Tbqhkmhynhw Iqwsjmovuibq Plwoglrv Lxrgpgwb Lublin Poland
Pueqszqfqbwvdlucpl Bielsko-Biala Poland
Kqokvrosrplvpu Pfbppx Dsq mtgl uerqh Wcgdgacf Jvcleplw Bad Homburg Germany
Krjcgngrznkciy Pqmnew ia Ssvrusjphp Berlin Germany
Pclni Seonsqphvue Ujuectprlj Hwdraigw Paris France
Nqqjqivyxgwdptv Zvlalpo Gepcxomwf Gog Goettingen Germany
Vvmllcko Chgwumdw Rdrvpfjk Gkpqarr Gzam Hamburg Germany
Uhgkvvejvtindfouboszi Crgg Giuxow Ccdab Dnadexj aq doy Tlwreauubao Uoisigslbzdt Dnomwgl Agb Dresden Germany
Icxilf Antwerp Belgium

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
23.11.2025
Belgium Belgium
Not recruiting
23.11.2025
Czechia Czechia
Not recruiting
23.11.2025
Denmark Denmark
Not recruiting
23.11.2025
France France
Not recruiting
23.11.2025
Germany Germany
Not recruiting
23.11.2025
Greece Greece
Not recruiting
23.11.2025
Hungary Hungary
Not recruiting
23.11.2025
Italy Italy
Not recruiting
23.11.2025
Poland Poland
Not recruiting
23.11.2025
Romania Romania
Not recruiting
23.11.2025
Slovakia Slovakia
Not recruiting
23.11.2025
Spain Spain
Not recruiting
23.11.2025
The Netherlands The Netherlands
Not recruiting
23.11.2025

Trial locations

Muvalaplin is a medication taken by mouth that is being tested to see if it can help reduce the risk of serious heart problems, such as heart attacks or strokes, in adults who have high levels of a specific type of protein in their blood called lipoprotein(a).

Investigated Diseases:

Elevated Lp(a) – This condition occurs when there is an unusually high level of Lipoprotein(a) in the blood. This substance is a type of particle that carries cholesterol through the bloodstream. Over time, high levels can contribute to the buildup of fatty deposits within the artery walls. This process can narrow the passages through which blood flows. The condition is often determined by genetic factors rather than lifestyle alone.

Atherosclerotic Cardiovascular Disease – This condition involves the buildup of fats, cholesterol, and other substances in and along the artery walls. This buildup is known as plaque. As the plaque grows, it can cause the arteries to become narrow and hard. This narrowing restricts the flow of oxygen-rich blood to various parts of the body. The condition typically progresses slowly over many years.

Trial ID:
2025-521067-13-00
Protocol code:
J2O-MC-EKBG
Trial Phase:
Therapeutic confirmatory (Phase III)

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