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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Other Sites

Site Name City Country Status
Pauls Stradins Clinical University Hospital Riga Latvia
University Multiprofile Hospital For Active Treatment Saint Georgi EAD Plovdiv Bulgaria
Hightech Medical Services S.R.L. Bucharest Romania
Hippokration Hospital Athens Greece
Consultmed S.R.L. Iasi Romania
KBC Zagreb Zagreb Croatia
Diagnostic & Therapeutic Center Of Athens Hygeia Single Member S.A. Athens Greece
MVZ CCB Frankfurt Und Main-Taunus GbR Frankfurt Germany
General University Hospital Of Larissa Larissa Greece
Klinikum Coburg GmbH Coburg Germany
University Of Debrecen Debrecen Hungary
Spitalul Clinic Judetean De Urgenta Bihor Oradea Romania
Università degli studi Gabriele D’Annunzio Chieti-Pescara Centro di Studi e tecnologie avanzate Chieti Italy
University General Hospital Of Thessaloniki Ahepa Thessaloniki Greece
Národny ustav srdcovych a cievnych chorob a.s. Bratislava Slovakia
Medical Center Hera EOOD Sofia Bulgaria
University General Hospital Of Ioannina Ioannina Greece
MHAT National Heart Hospital EAD Sofia Bulgaria
Uniwersytecki Szpital Kliniczny W Bialymstoku Bialystok Poland
Spitalul Clinic Municipal De Urgenta Timisoara Timisoara Romania
Nemocnice Slany Slany Czechia
Mat Cord Biomedica S.R.L. Buzau Romania
Kresmed Sp. z o. o. Ostrow Mazowiecka Poland
Saules seimos medicinos centras UAB Kaunas Lithuania
ClinPhenomics CVC GmbH Frankfurt Germany
Sal Med S.R.L. Pitesti Romania
Diagnostic-consultative center “Aleksandrovska” EOOD Sofia Bulgaria
Odense University Hospital Odense Denmark
Ospedale San Raffaele S.r.l. Milan Italy
Fondazione IRCCS Policlinico San Matteo Pavia Italy
Region Skane Skanes Universitetssjukhus Lund Sweden
Universita’ Degli Studi Di Verona Verona Italy
Alexandra Hospital Athens Greece
Charite Universitaetsmedizin Berlin KöR Berlin Germany
Karolinska University Hospital Solna Sweden
Az St-Jan Brugge-Oostende A.V. Brugge Belgium
Saarland University Hospital Homburg Germany
Hospital Universitario De Cruces Barakaldo Spain
IRCCS Ospedale Policlinico San Martino Genoa Italy
University Clinical Hospital Virgen De La Arrixaca Murcia Spain
Sygehus Lillebaelt Vejle Sygehus Vejle Denmark
Spitalul Universitar De Urgenta Bucuresti Bucharest Romania
Aalborg University Hospital Aalborg Denmark
Spitalul Clinic Judetean De Urgenta Sfantul Apostol Andrei Constanta Constanta Romania
Centrum Badan Klinicznych Piotr Napora Lekarze sp.p. Wroclaw Poland
General University Hospital Of Patras Patras Greece
Belvarosi Egeszseghaz Kft. Zalaegerszeg Hungary
Cardiomobile Kft. Balatonfured Hungary
Ko-Med Centra Kliniczne Sp. z o.o. Zamosc Poland
Medical Center – University Of Freiburg Freiburg Im Breisgau Germany
Zaans Medisch Centrum Stichting Zaandam The Netherlands
University General Hospital Of Alexandroupoli Alexandroupoli Greece
Centro Hospitalar Do Baixo Vouga E.P.E. (CHBV E.P.E.) Aveiro Portugal
Bravis Ziekenhuis Roosendaal The Netherlands
Centro Hospitalar de Setubal E.P.E. Setubal Portugal
Region Midtjylland Aarhus Denmark
University Of Szeged Szeged Hungary
American Heart Of Poland S.A. Kedzierzyn-Kozle Poland
University Multiprofile Hospital For Active Treatment St. Ivan Rilski EAD Sofia Bulgaria
Pirmoji Viltis UAB Siauliai Lithuania
Uniwersytecki Szpital Kliniczny W Poznaniu Poznan Poland
Kardiomed Nz s.r.o. Nove Zamky Slovakia
Jahn Ferenc Del-Pesti Korhaz Es Rendelointezet Budapest Hungary
Ziekenhuis Oost Limburg Genk Belgium
Poliklinika Solmed d.o.o. Zagreb Croatia
Gelre Hospitals Zutphen The Netherlands
Klaipedos universiteto ligonine VšĮ Klaipeda Lithuania
Salve Medica Sp. z o.o. S.K. Lodz Poland
Noordwest Ziekenhuisgroep Stichting Alkmaar The Netherlands
Centro Cardiologico Monzino S.p.A. Milan Italy
Azienda Ospedaliero-Universitaria Sant Andre Rome Italy
Region Oerebro Laen Orebro Sweden
Algemeen Ziekenhuis Klina Brasschaat Belgium
APDP Associacao Protectora Dos Diabeticos De Portugal Lisbon Portugal
Universitaetsklinikum Aachen AöR Aachen Germany
Universitaetsklinikum Schleswig-Holstein AöR Kiel Germany
Centre Hospitalier Regional De La Citadelle Liege Belgium
Hospital Universitario Puerta De Hierro De Majadahonda Majadahonda Spain
Elias University Emergency Hospital Bucharest Romania
Amphia Hospital Breda The Netherlands
Unidade Local De Saude De Gaia/Espinho E.P.E. Vila Nova De Gaia Portugal
Narodowy Instytut Kardiologii Stefana Kardynala Wyszynskiego Panstwowy Instytut Badawczy Warsaw Poland
Azienda Ospedaliera Universitaria Policlinico Paolo Giaccone Palermo Italy
Universita Degli Studi Di Brescia Brescia Italy
Universita’ Degli Studi Di Ferrara Ferrara Italy
University Hospital Bratislava Bratislava Slovakia
Tergooiziekenhuizen Hilversum The Netherlands
Queen Silvia Childrens Hospital – Sahlgrenska University Hospital – Vaestra Goetalandsregionen Gothenburg Sweden
Instytut Centrum Zdrowia Matki Polki Lodz Poland
Lietuvos sveikatos mokslu universiteto ligonine Kauno klinikos Kaunas Lithuania
Adoria SIA Riga Latvia
University Hospital St Marina Varna Varna Bulgaria
Azienda Unita Locale Socio Sanitaria N 8 Berica Vicenza Italy
Geniko Nosokomeio Thessalonikis George Papanikolaou Thessaloniki Greece
InnoDiab Forschung GmbH Essen Germany
Algemeen Ziekenhuis Groeninge Kortrijk Belgium
R.E.D. Institut fuer medizinische Studien und Fortbildung GmbH Oldenburg In Holstein Germany
Komaromi Selye Janos Korhaz Komarom Hungary
CCAB Centro Clinico Academico Braga Associacao Braga Portugal
Thermi Clinic S.A. Thessaloniki Greece
University General Hospital Of Heraklion Heraklion Greece
Samodzielny Publiczny Specjalistyczny Szpital Zachodni Im.Sw.Jana Pawla II Grodzisk Mazowiecki Poland
Hospital Universitario Dr Peset Aleixandre Valencia Spain
Algemeen Ziekenhuis Damiaan Oostende Ostend Belgium
Cardio Med S.R.L. Craiova Romania
Diamed Obesity S.R.L. Galati Romania
Institutul De Boli Cardiovasculare Timisoara Timisoara Romania
Daugavpils regionala slimnica SIA Daugavpils Latvia
Unidade Local De Saude Do Alto Minho E.P.E. Ponte De Lima Portugal
Gottsegen National Cardiovascular Center Budapest Hungary
Medyczne Centrum Diabetologiczno-Endokrynologiczno-Metaboliczne Diab-Endo-Met Sp. z o.o. Cracow Poland
Hospital Virgen De Las Montanas Villamartin Spain
ARNAS Civico Di Cristina Benfratelli Palermo Italy
Medical group Kosice s.r.o. Kosice Slovakia
D & A Research B.V. Sneek The Netherlands
Ziekenhuisgroep Twente Stichting Almelo The Netherlands
Acibadem City Clinic University Multiprofile Hospital For Active Treatment EOOD Sofia Bulgaria
Hospital Virgen Del Camino Sanlucar De Barrameda Spain
Ziekenhuis St Jansdal Harderwijk The Netherlands
Unidade Local De Saude De Matosinhos E.P.E. Senhora Da Hora Portugal
Edumed s.r.o. Nachod Czechia
Spitalul Judetean De Urgenta Braila Braila Romania
Kalthus Heart & Horse AB Lund Sweden
Мultidisciplinary hospital for active treatment Saint George Pernik OOD Pernik Bulgaria
Ikazia Ziekenhuis Rotterdam The Netherlands
Uniwersytecki Szpital Kliniczny Nr 2 Uniwersytetu Medycznego W Lodzi SPZOZ Lodz Poland
Kaunas city polyclinic Public institution Kaunas Lithuania
Specijalna Bolnica Za Medicinsku Rehabilitaciju Krapinske Toplice Krapinske Toplice Croatia
Multi-profile Hospital for Active Treatment Heart and Brain EAD Pleven Bulgaria
Emergency Institute For Cardiovascular Diseases And Transplant Targu Mures Romania
Diabeda s.r.o. Bratislava Slovakia
Facharztzentrum Dresden-Neustadt Betriebsgesellschaft mbH Dresden Germany
Davius Clinicmed S.R.L. Bucharest Romania
Bella Praxis S.R.L. Pascani Romania
General Hospital Of Nea Ionia Konstantopouleio Patision Nea Ionia Greece
Lotus Med S.R.L. Bucharest Romania
Respublikine Panevezio ligonine VšĮ Panevezys Lithuania
Narodny Endokrinologicky A Diabetologicky Ustav Lubochna Slovakia
MEDICON a.s. Prague Czechia
Cardioconsult s.r.o. Stare Mesto Slovakia
Diamedical Medical Center 2013 Ltd. Dimitrovgrad Bulgaria
St. Josefskrankenhaus Heidelberg GmbH Heidelberg Germany
Medical Center New Rehabilitation Center EOOD Stara Zagora Bulgaria
Marienhaus Klinikum Mainz GmbH Mainz Germany
Universitätsklinikum des Saarlandes – Homburg/Saar, Klinik für Urologie und Kinderurologie Homburg Germany
Region Sjaelland Holbæk Denmark
Vital s.r.o. Levice Slovakia
Fakultna Nemocnica S Poliklinikou J. A. Reimana Presov Presov Slovakia
Azorg Aalst Belgium
University General Hospital Attikon General Hospital Of West Attica H Agia Varvara Chaidari Greece
Azienda Ospedaliero Universitaria Pisana Pisa Italy
Azienda Sanitaria Universitaria Giuliano Isontina Trieste Italy
Centermed Sp. z o.o. Lublin Poland
Medical KG s.r.o. Piestany Slovakia
Zentrum für klinische Studien Südbrandenburg GmbH Elsterwerda Germany
Centrum Kliniczno-Badawcze J.Brzezicki B.Gornikiewicz-Brzezicka Lekarze sp.p. Elblag Poland
Safsaikvhafgsdm Giaviik Dyomkwddzopysqz Rjpxtzby Rvzplqtdlvp Gorzów Wielkopolski Poland
Lvrpq Gedzjvu Hublcmls Oc Aajuet Athens Greece
Cer Djz Peyvfmaci Czlnpbdy Targu Mures Romania
Ivkvvszfyq dm Bzhy Cvxxwndcdtsdzsy &wbooznhvzzm Dqx Gfmwql Iovb Gbiyzsdqbxaqmxxz Izoa Iasi Romania
Dlxufy Copflapv Rntdvvdx Dczuooeljri Gdmc Duesseldorf Germany
Myynuiw Cbhads Bnbgqhao Lkzo Yambol Bulgaria
Zvltftxw dycfrey cppfyj Sxl Jelgava Latvia
Prrnyld Mdhecy Set z Obnb Edr Pqhrabtra Poniatowa Poland
Scw Kbdyksyo Kdnnqhvabgmhonqengaadtfc Gpis Karlsbad Germany
Peskmplnh 2xwj Mqasz Stara Zagora Bulgaria
Koprwi Lglq Gdansk Poland
Irgfob sppbrh Presov Slovakia
Khyliiftmje Snphixzibz Uxa Kaunas Lithuania
Gfqvrfm Hdbruaca Os Tgvsgpkbuoft Axcwu Pxzeyj Kalamaria Greece
Igxouzlie skitjs Nitra Slovakia
Cxyfivh Mbdkhhr Ilncaaekhe dk Cfnzzbofzgr Dal Ptp Cgsds Baia Mare Romania
Zaeojbr Surn Apladegbd i Dpjlvf Dinhjd Wroclaw Poland
Smchytobdlzlsdx Pqotggdv Lhdqpynw Ekq Makfapjunhhgmzta Cracow Poland
Mtbkpzv Ctirpw Insb Tmmxippx Ybokrw Evfg Sofia Bulgaria
Kzigejlm bpcsuveo cwilti Rwunpa (bxeldmvp Hzqfziem Cxopxt Rvjhclu Rijeka Croatia
Dgcesezwok Cqlrecgedjxm Cumcgo (nsbz &npohwfynibf Atnesozkodx Eers Sofia Bulgaria
Ewkygrynqqvqk Brm Baja Hungary
Zjvacsl frl koxrxzpvh Faxlpqgllo Dkg mjkf Linbhund Falkensee Germany
Alr Mpp Lzkb Daugavpils Latvia
Dwmsx Myhszxj Srlarw Bucharest Romania
Cemakxl Mxowhhm Ewvvtji Bxgxhgfdw Bucharest Romania
Ncxyhgtyl Mberyzk Szclh Craiova Romania
Mwwdtaf Ccbsuu Mtbu Cvag Omj Kyustendil Bulgaria
Sdmzrwj Pgfntldzp ipi Hbybyvcl Sstyklarxz Layotdyfiejl Scftltpokyn Pn Zgmyuj Oqrcbf Zajfvexto Węgrów Poland
Przxuxfp Lpmpyxaw Mcadecp Seipg Cracow Poland
Clzfmij Mpdtbrun Vlfw Psmnlpkc Kzqadnduioskcc Szczecin Poland
Sjxipeuikpogsax Pyxqbewo Lgkagcni w Oculkhuoqvz Ogrodzieniec Poland
Pgalxk Rtfqigcqumtl Reichelsheim Germany
Uvrwxqf Ugogsurhjh Hhpzxnhh Uppsala Sweden
Auyjhij Ozqgzlplyki Pyy Lpadjsoxggkheaqds Cbhbblziet Catania Italy
Akftxr Uissodhgze Htuqouaf Aarhus Denmark
Ctxufa Hykkqutkjb E Uoefuhxfsywyl Dl Cxjqbwj Eswzpq Coimbra Portugal
Rimhi Aylzgclq klqhyrhi ukynqxjoanvbl sijlpndf Sob Riga Latvia
Aqifbbqye Umn Amsterdam The Netherlands
Inwgkcfh Uno Kaunas Lithuania
Axlxhn Mvjdqsn Cheaez Szyh Thessaloniki Greece
Gbmnsl Ujjhqkcunb Fhoxopboc Frankfurt Germany
Aatxlnm Cqfdesh Scy z owul Scqx Ruda Slaska Poland
Srzcvckt Crzqfa Da Udasxwe Sbtflvj Bucharest Romania
Avonxmg Uptbf Sozcebwxw Liccke Dr Bvydzfb Bologna Italy
Ahztafm Oxqykpqdcnb Ppel Gpzhexwj Xpjdy Bergamo Italy
Ieezcydth Fnw Czaehnmt Avu Ekwxpmktqbcj Mmjjnxuy Prague Czechia
Hzdneqhf Hydbvpzp Hvidovre Denmark
Mqjtbujxsynfurzdsmdmyhdwxx Hphrhoqwsqcohadh Halle (Saale) Germany
Uuaktshgch Mltgj Gdbutrg Oc Cuexroitj Catanzaro Italy
Ctwvuol Mhmqiol Dv Dwmchshcdd Sb Trxntcyvr Arvmwcamo Nxejiw Sjhkvf Brasov Romania
Islawy Bonheiden Belgium
Ereaose Mechelen Belgium
Ccysoz Hfgfuqjkfn Dd Tvkdmw E Smjxl Emxpnz Guilhufe Portugal
Pvirbjmojz Kcnl Bekescsaba Hungary
Gbovxyh Hxlvgtdw Oy Ctpef Slzxvtwkyi Chios Greece
Msopfgo Ckykmr Mqwindxigj Pqzhjc Oaa Pleven Bulgaria
Ibzhdwbrwusm Szjehlrbtkcztip Phahsyki Lvvjizfc w djhjmvxkkm klprwjzliyw Lwd mstn Kikxgnpsi Czbkkgjb Gdynia Poland
Cztuexjf Hijzfgzs Dshgphl Zagreb Croatia
Kmqbpmvkv Suxjohr Snipeybaxapkauh ib Jnay Pmfil Id Cracow Poland

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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