A study of ziltivekimab compared to placebo in people with heart and blood vessel disease, chronic kidney disease and inflammation

3 1

What is this study about?

This study examines people with atherosclerotic cardiovascular disease, chronic kidney disease, and systemic inflammation. Atherosclerotic cardiovascular disease is a condition where fatty deposits build up in the arteries, which can affect blood flow to the heart, brain, or limbs. Chronic kidney disease means the kidneys are not working as well as they should, which affects their ability to filter waste from the blood. Systemic inflammation refers to widespread inflammation in the body that can be measured through blood tests. The study compares the effects of ziltivekimab, an experimental medication given as an injection under the skin once a month, with placebo. Both treatments are given in addition to the usual care that patients receive for their conditions.

The purpose of the study is to see if ziltivekimab works better than placebo in reducing the risk of serious heart-related problems in people who have both cardiovascular disease and kidney disease along with signs of inflammation in their body. The main focus is on preventing major cardiovascular events, which include death from heart-related causes, non-fatal heart attack, and non-fatal stroke. A heart attack occurs when blood flow to part of the heart muscle is blocked, while a stroke happens when blood flow to part of the brain is interrupted.

During the study, participants will receive either ziltivekimab or placebo through regular injections while continuing their standard medical treatment. The study will track various health outcomes over time, including heart attacks, strokes, heart-related deaths, hospital admissions for heart problems, and changes in kidney function. Researchers will also monitor changes in inflammation markers in the blood, heart function measurements, and overall health status. The study will measure how the kidneys are working by looking at blood test results that show the filtering ability of the kidneys and the amount of protein in the urine, which can indicate kidney damage.

1 Assignment to treatment group

Upon entering the study, you will be randomly assigned to receive either ziltivekimab or placebo. This assignment is done by chance, similar to flipping a coin.

The placebo looks identical to ziltivekimab but contains no active medication. This helps researchers determine if the study medication is effective.

Both ziltivekimab and placebo will be given in addition to your standard medical care, which means you will continue taking your regular medications as prescribed by your doctor.

2 Monthly injections

You will receive injections under the skin (subcutaneous injections) once every month throughout the study.

The medication is provided as a solution for injection, which means it is a liquid ready to be injected.

These monthly injections will continue for the entire duration of the study.

3 Regular monitoring visits

During the study, you will attend regular visits where various measurements and tests will be performed.

Blood samples will be taken to measure specific markers in your blood, including hs-CRP (a marker of inflammation in your body), NT-pro-BNP (a marker related to heart function), and haemoglobin (a component of blood that carries oxygen).

Your kidney function will be monitored by measuring eGFR (estimated glomerular filtration rate, which shows how well your kidneys are filtering waste from your blood) and UACR (urine albumin-to-creatinine ratio, which detects protein in your urine).

These measurements will be taken at the beginning of the study and repeated at specific time points, including at 2 years into the study.

4 Heart function assessment

Your heart function will be evaluated by measuring left ventricular ejection fraction, which indicates how well the main pumping chamber of your heart is working.

This measurement will be taken at the start of the study and again at 2 years.

5 Quality of life assessment

You will be asked to complete a questionnaire called Short Form 36, which assesses your physical health and how it affects your daily activities.

This questionnaire will be completed at the beginning of the study and at 2 years.

6 Ongoing health monitoring

Throughout the study, any health events will be recorded, including heart-related events such as heart attack (myocardial infarction), stroke, cardiovascular death (death related to heart or blood vessel problems), hospitalizations for heart failure, and procedures to restore blood flow to the heart or other arteries.

Kidney-related events will also be monitored, including significant decreases in kidney function or the need for kidney replacement therapy (such as dialysis or kidney transplant).

Any episodes of atrial fibrillation (irregular heart rhythm) will be documented.

Hospitalizations or deaths related to infections will be recorded.

All deaths from any cause will be tracked.

7 Continuation until study completion

You will continue receiving the monthly injections and attending monitoring visits until the study ends.

The study is expected to continue for several years, and the exact end date will be determined by the research team based on the number of health events observed across all participants.

Who Can Join the Study?

  • You must have chronic kidney disease, which means your kidneys do not work as well as they should. This can be shown in one of two ways: either your eGFR (a blood test that measures how well your kidneys filter waste) is between 15 and 60, or your UACR (a urine test that measures protein in your urine) is 200 or higher with an eGFR of 60 or above.
  • Your blood test must show a hs-CRP level of 2 or higher. This measures inflammation in your body, which means there is swelling or irritation inside your body that you may not be able to feel.
  • You must have atherosclerotic cardiovascular disease, which means you have hardening and narrowing of your blood vessels. This can be shown by having one or more of the following conditions:
  • You have coronary heart disease, which affects the blood vessels of your heart. This includes having had a heart attack in the past, having had a procedure to open blocked heart arteries, or having at least 50% blockage in a major heart artery shown by special imaging tests.
  • You have cerebrovascular disease, which affects the blood vessels in your brain and neck. This includes having had a stroke caused by blocked arteries, having had a procedure to open blocked neck arteries, or having at least 50% blockage in a neck artery shown by special imaging tests.
  • You have symptomatic peripheral artery disease, which affects the blood vessels in your legs and causes symptoms. This includes having leg pain when walking with an ankle-brachial index of 0.90 or less (a test comparing blood pressure in your ankle and arm), having leg pain with at least 50% blockage in leg arteries shown by special imaging tests, having had a procedure to open blocked leg arteries, or having had part of your leg amputated due to blocked arteries.
  • You must be an adult.
  • Both men and women can participate in this study.

Who Cannot Join the Study?

  • The study does not list specific reasons why patients cannot participate in the trial based on the available information
  • If you have questions about whether you can join this study, your doctor will need to review the complete study requirements with you
  • General factors that often prevent participation in clinical trials may include having certain other medical conditions, taking specific medications, or having recent surgeries, but these have not been specified for this particular study
  • Your healthcare provider will determine if you meet all the necessary requirements to safely participate in this research

Where you can join this trial?

Verified and Recommended Sites

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Verified Sites

Other Sites

Site Name City Country Status
Diagnostic & Therapeutic Center Of Athens Hygeia Single Member S.A. Athens Greece
Ospedale San Raffaele S.r.l. Milan Italy
Karolinska University Hospital Solna Sweden
Sygehus Lillebaelt Vejle Sygehus Vejle Denmark
Spitalul Universitar De Urgenta Bucuresti Bucharest Romania
Amphia Hospital Breda The Netherlands
MVZ CCB Frankfurt Und Main-Taunus GbR Frankfurt Germany
Klinikum Coburg GmbH Coburg Germany
Spitalul Clinic Municipal De Urgenta Timisoara Timisoara Romania
Sal Med S.R.L. Pitesti Romania
Universitätsklinikum des Saarlandes – Homburg/Saar, Klinik für Urologie und Kinderurologie Homburg Germany
Vital s.r.o. Levice Slovakia
Az St-Jan Brugge-Oostende A.V. Brugge Belgium
Saarland University Hospital Homburg Germany
Hospital Universitario De Cruces Barakaldo Spain
Centrum Badan Klinicznych Piotr Napora Lekarze sp.p. Wroclaw Poland
University Multiprofile Hospital For Active Treatment St. Ivan Rilski EAD Sofia Bulgaria
Uniwersytecki Szpital Kliniczny W Poznaniu Poznan Poland
Klaipedos universiteto ligonine VšĮ Klaipeda Lithuania
Centre Hospitalier Regional De La Citadelle Liege Belgium
Instytut Centrum Zdrowia Matki Polki Lodz Poland
University Hospital St Marina Varna Varna Bulgaria
Gottsegen National Cardiovascular Center Budapest Hungary
Hospital Virgen De Las Montanas Villamartin Spain
ARNAS Civico Di Cristina Benfratelli Palermo Italy
Specijalna Bolnica Za Medicinsku Rehabilitaciju Krapinske Toplice Krapinske Toplice Croatia
Narodny Endokrinologicky A Diabetologicky Ustav Lubochna Slovakia
Cardioconsult s.r.o. Stare Mesto Slovakia
St. Josefskrankenhaus Heidelberg GmbH Heidelberg Germany
Azorg Aalst Belgium
Hqryaxtggjyh Habobzfe Athens Greece
Gcemlui Uuvubuomzw Hjyzoehs Oz Leucwup Larissa Greece
Uhttxgucqo Ou Dxipevwy Debrecen Hungary
Lzlis Gcwkmgy Hezqwhrf Oy Awoccd Athens Greece
Ujyvexnatb Geoliiu Hwdvfdpy Oz Tqitcblwfjei Auhbu Thessaloniki Greece
Mqtwcsb Cjmzgj Hzab Ecre Sofia Bulgaria
Ugqmzpowxd Gvggxic Hbrpvhlw Oo Ivbprtug Ioannina Greece
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Rvyucv Sqyrsguww Holbæk Denmark
Otlamc Unjzqclion Hsnsfiak Odense Denmark
Fgdeezxlhv Ihizr Paunvucovpf Siq Mcmvvd Pavia Italy
Rkkomb Sudoi Shigzu Usrukxeyjabfqatklld Lund Sweden
Umxprnmodntwnufqb Djxmm Sayky Dl Vjjojc Verona Italy
Atxzksxmv Hkcavild Athens Greece
Uclzgzh Uktqnmglel Htmhasek Uppsala Sweden
Czogiei Uyilacmgxonjkgivrcqp Bqjxqp Kov Berlin Germany
Iorme Oqixfaph Ptfgyfjykba Sdo Mdgoqbb Genoa Italy
Uwuvfnidms Cfjsmsgt Hmttcqsv Vgzvfq Dl Lt Akoiaxnp Murcia Spain
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Gmfpuar Ubhzqvjjxl Hqmlphif Og Plntsf Patras Greece
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Mceyabq Cntzfk &rewtzx Ufqhlfadsp Oh Fvqazjzf Freiburg Im Breisgau Germany
Awcxhb Mbivqce Cjcokx Slsx Thessaloniki Greece
Ucqkchkkhc Gblfbjb Hpojmdai Og Awhhxllqtoyuhe Alexandroupoli Greece
Rpajgw Musjplwpcuz Aarhus Denmark
Undfsznawk Oi Sfregl Szeged Hungary
Axnidpa Umblx Scilkbsvf Lffdce Dg Bokoqai Bologna Italy
Phrnqlrhrcb Snrgtt dzfoqj Zagreb Croatia
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Rjniww Octkkev Lvys Orebro Sweden
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Sriililoqntfmbo Grifgny Dtxkbpxomjfzyet Rdiapprc Rykuupslohm Gorzów Wielkopolski Poland
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Uxhvccsmyt djigx sndoe Ggqefzmx Dakiwvlihy Ctuievlqtdoyaw Cjpgbj du Spffh e tdlbncgnkh axbcvael Chieti Italy
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Cbg Dgp Psjvmvfis Czxhzpkv Targu Mures Romania
Ibkaadopdp dt Bako Cgiznslaynqlexx &mahrdqrswbo Dqn Gnpwxq Ingw Gnnljtsfuefwcbun Ipcn Iasi Romania
Mdnq Nghdhlrv Hgpvd Hjjjgptw Ezy Sofia Bulgaria
Uujphuuaqroff Swmmjey Klkfncvuj W Bqootuqbfqx Bialystok Poland
Doguvb Cyhaucqd Rzmiegmf Dqlbzqaubcu Gcmg Duesseldorf Germany
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Ctoetpgxcheqy Csu Gqzf Frankfurt Germany
Cfepyfg Mfbgtaq Ifnjnyziza dr Cjglkgefmlv Dmy Ply Cphny Baia Mare Romania
Zqcvrmz Siaq Amvadtmup i Dcpgdv Diwvxw Wroclaw Poland
Svphlftnhyetrxq Plczkccn Lurxymcl Eqx Mvydiudmvvnzcpvp Cracow Poland
Maewmjk Ctkayw Iaea Tgzhrhuz Yjikgr Ephn Sofia Bulgaria
Keazuixi bakhzzkz cewgwq Rkeqwu (bxjlbjpe Hmvddfkv Cqqqdc Rhjwbah Rijeka Croatia
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Eqrabrhmkkitx Byo Baja Hungary
Zbsilec fvl kdtnjpniw Fyrcjqbqmy Dss maqm Lilgqpuy Falkensee Germany
Aup Mmc Lkop Daugavpils Latvia
Dzhwo Mcvtmxq Sgvrgk Bucharest Romania
Cpomrze Mmwdepa Epeqmpu Boydxmadz Bucharest Romania
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Msvhgve Cijygn Mlfc Ckgt Ovo Kyustendil Bulgaria
Sbaeiyv Pmoxoozvh ife Hpknrjne Sgnlcqqhqn Lhsmznrqiank Spikkcyihkc Pn Zadghu Oxbkfn Zupjcnhen Węgrów Poland
Pidwbjzh Lficyrcy Mhxypyy Sveoe Cracow Poland
Cvppfpa Mxjfqqgw Vypj Ptdhavxo Kccycnadmsfnws Szczecin Poland
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Pyntvc Rqdcxrfkesym Reichelsheim Germany
Apjijmc Octysvjxuax Pgz Ldtyubtanzbmwifwi Clircvfjmz Catania Italy
Aummjl Uxfxlzzjms Hymtftke Aarhus Denmark
Rfsri Ahlmarrd kazdfuar uwnsrbkzfjbwp skapxbvs Srp Riga Latvia
Selrdngf Ccplyd Jxjphyhh Dl Ujhbtui Srysxmh Amdbziy Akrstl Cmtwdltgs Constanta Romania
Abhokkhwf Uzq Amsterdam The Netherlands
Bwxqoxdbx Eaepxqgejho Khza Zalaegerszeg Hungary
Ctairvphmlzu Kius Balatonfured Hungary
Kfjqzr Cahyvp Kjbbeeyxl Smy z oxre Zamosc Poland
Zvosc Mlmmtmn Cehfxpr Srnfxctrc Zaandam The Netherlands
Gsnvho Uzbyrbiipj Ftufgwowh Frankfurt Germany
Cjornc Hiluthtuki Dx Bfqah Vrvna Epmwmy (xwiv Eercspc Aveiro Portugal
Bgdqdv Zcglbmpmve Roosendaal The Netherlands
Cxpwuo Hwbiquvvof dx Swfwciz Exdrnh Setubal Portugal
Alfebgbs Hpbrd Of Psxmop Shqb Kedzierzyn-Kozle Poland
Ayfgkpf Cjgpjlv Spi z oasi Skxo Ruda Slaska Poland
Pmxvqpb Vxyzfq Uyv Siauliai Lithuania
Kzgveswjc Nb scnnvi Nove Zamky Slovakia
Jrye Frkjku Dqimymnlu Kybylr Ep Roaoyxxzjombqo Budapest Hungary
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Zqkqjtoimw Owss Ltlbcrd Genk Belgium
Goqqz Hzomsrndk Zutphen The Netherlands
Sirrh Mpwpgi Sxz z okli Scsj Lodz Poland
Nnwetuzsl Zecmgsowofsothz Sksveqtqw Alkmaar The Netherlands
Cmokgj Ckzdsbrtkgez Mfnqweq Sazjqy Milan Italy
Asyoodn Otxixjeimpcxexrewegobaaaf Saux Aeorq Rome Italy
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Hlvtinwi Hdebfjqi Hvidovre Denmark
Mjkifwemopbjjqjqciwgihmepd Hbppebjvviyaovkd Halle (Saale) Germany
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Uoygdcs Lctjy Dg Slacp De Gmryapbltknd Emjavg Vila Nova De Gaia Portugal
Nvzoztsy Ihegjlfy Kanlfjynpcf Sgmnmxz Knywevayo Wbueiqryhspo Puvkmkaoi Iofzpcgc Blwroxpf Warsaw Poland
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Teupghkcavckszounze Hilversum The Netherlands
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Aexxkh San Riga Latvia
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Ifwukf Bonheiden Belgium
Irfegszw Flzjfqswj Gwhe Essen Germany
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Ekgzeow Mechelen Belgium
Kdqlncxq Sdktb Jviqw Kpdmml Komarom Hungary
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Ckjmma Mke Sxpsos Craiova Romania
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Daurohglec rrjttmepa snmcipry Sou Daugavpils Latvia
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Memzzsno Ckcoqxl Dskdwvstupipoxfklcmxlljghuvscvikthyfqdipurbfrg Dkdlfnbauhlox Suv z oxts Cracow Poland
D &qrge A Rwjhampl Bktr Sneek The Netherlands
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Agoltzao Czks Cuphwq Ulsizlcqsi Mgnomfifpprp Hjlhidqs Fym Abcpyc Tihzyfqry Erwe Sofia Bulgaria
Hwrsrxem Vzbsze Dfo Cfhwru Sanlucar De Barrameda Spain
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Dlaunk Cbjjjhmbs Sopiaz Bucharest Romania
Gykpwtv Hpqaymmy Oq Cfkst Sabnvqglej Chios Greece
Bcbaj Pzcyba Sixjdu Pascani Romania
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Lcwag Mtd Sqcjcs Bucharest Romania
Rhpbihohlhec Pafrfpgqt lfkjrxcp Vgw Panevezys Lithuania
Mkuodrp azuw Prague Czechia
Dybxhmqmza Moejvgo Cwwpps 2uld Lymv Dimitrovgrad Bulgaria
Mccayej Cpkrjx Nur Reozdjgmlohipl Chwxkp Eabu Stara Zagora Bulgaria
Mkfopzsrbf Kcbwfova Muqzq Ggpv Mainz Germany
Iwvqaethzphm Sqyjhcodbibqily Puaizgpl Llebhfkw w dvjuaacngg krnwgbaryyd Lbe mekr Kfiygeeqf Cimrltkg Gdynia Poland
Ctjbppwv Hapzfcbk Ddrmeei Zagreb Croatia
Cbtvukbwt Sdw z ozve Lublin Poland
Fleijmmu Nexxrmxim S Pxxnyxaguamy Jw Aw Rqpzkiw Pxrseh Presov Slovakia
Ksnrwfslb Sknilne Sunmeakmebgtkhy iv Jozo Pctfx Iw Cracow Poland
Amxwxer Sjhjcbsus Ukbtmlkcxrebz Gghdekls Idsirgvm Trieste Italy
Clcokop Kaggrpfqgddubcpery Jrchcbdthmm Bkbamjvshaijnkkzgecgtegx Ltzsmlx sqvxn Elblag Poland
Mvikmmv Ki stnyjg Piestany Slovakia
Zokhspd fqb kdmqyhfdw Sjvlnmn Sjdtkrqggpzrfw Gsus Elsterwerda Germany

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

Trial status

Country Status Recruitment Start
Belgium Belgium
Not recruiting
01.09.2021
Bulgaria Bulgaria
Not recruiting
01.09.2021
Croatia Croatia
Not recruiting
01.09.2021
Czechia Czechia
Not recruiting
01.09.2021
Denmark Denmark
Not recruiting
01.09.2021
Germany Germany
Not recruiting
01.09.2021
Greece Greece
Not recruiting
01.09.2021
Hungary Hungary
Not recruiting
01.09.2021
Italy Italy
Not recruiting
01.09.2021
Latvia Latvia
Not recruiting
01.09.2021
Lithuania Lithuania
Not recruiting
01.09.2021
Poland Poland
Not recruiting
01.09.2021
Portugal Portugal
Not recruiting
01.09.2021
Romania Romania
Not recruiting
01.09.2021
Slovakia Slovakia
Not recruiting
01.09.2021
Spain Spain
Not recruiting
01.09.2021
Sweden Sweden
Not recruiting
01.09.2021
The Netherlands The Netherlands
Not recruiting
01.09.2021

Trial locations

Investigated Drugs:

Ziltivekimab is an investigational medication given as an injection under the skin once a month. It is being tested to see if it can reduce the risk of major heart problems in people who have heart disease, kidney disease, and inflammation in their body. This medication is given in addition to the standard treatments that patients are already receiving for their conditions.

Placebo is an inactive substance that looks like the real medication but contains no active medicine. It is used in this study to compare against ziltivekimab to help determine if the real medication is working. Patients receiving placebo will also continue to receive their standard care treatments.

Atherosclerotic Cardiovascular Disease – Atherosclerotic cardiovascular disease is a condition where fatty deposits called plaques build up inside the arteries that supply blood to the heart and other parts of the body. These plaques are made up of cholesterol, fat, calcium, and other substances found in the blood. Over time, the plaques harden and narrow the arteries, reducing blood flow to vital organs. As the disease progresses, the plaques can rupture or break open, leading to blood clot formation. This reduced blood flow can cause chest pain, shortness of breath, and may lead to serious events such as heart attacks or strokes. The condition develops gradually over many years and often shows no symptoms in its early stages.

Chronic Kidney Disease – Chronic kidney disease is a long-term condition where the kidneys gradually lose their ability to filter waste products and excess fluids from the blood. The kidneys become damaged over time due to various factors such as high blood pressure, diabetes, or other underlying health conditions. As the disease progresses, waste products and fluids build up in the body, which can cause various health problems. The kidney function is measured by a value called estimated glomerular filtration rate, which decreases as the disease worsens. In advanced stages, the kidneys may lose most of their filtering ability, requiring medical intervention to remove waste from the blood. The progression of the disease is typically divided into five stages, with stage five being the most severe.

Systemic Inflammation – Systemic inflammation is a condition where the body’s immune system remains activated throughout the entire body rather than just in a specific area. This widespread immune response causes the release of inflammatory substances into the bloodstream that affect multiple organs and tissues. The inflammation persists over time and can be measured through blood tests that detect markers such as C-reactive protein. This ongoing inflammatory state can contribute to damage of blood vessels and organs throughout the body. The condition often occurs alongside other diseases and can worsen their progression. Unlike acute inflammation that resolves quickly, systemic inflammation continues for extended periods and becomes a chronic health issue.

Trial ID:
2023-506926-35-00
Protocol code:
EX6018-4758
Trial Phase:
Therapeutic confirmatory (Phase III)

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