Study of BI 690517 and empagliflozin combination for protection of heart and kidneys in patients with chronic kidney disease

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What is this study about?

This clinical trial focuses on chronic kidney disease and tests a combination of two medications. The first medication is BI 690517, an aldosterone synthase inhibitor, and the second is empagliflozin (also known as Jardiance), which belongs to a group of medicines called SGLT2 inhibitors. The study aims to determine if taking BI 690517 daily together with empagliflozin can help prevent the worsening of kidney disease, reduce hospitalizations due to heart problems, or prevent death from heart disease in people with kidney disease.

The study uses film-coated tablets that participants take by mouth. Some participants will receive BI 690517 together with empagliflozin, while others will receive a placebo tablet together with empagliflozin. The treatment period will last for up to 48 months. The study is designed to be double-blind, which means neither the participants nor the doctors know who receives which treatment.

During the study, doctors will monitor kidney function and heart health through regular medical examinations. They will track any changes in kidney function, instances of hospitalization, and other important health events. This information will help determine how effective the combination of medications is in protecting both the kidneys and heart in people with chronic kidney disease.

1 Initial medication phase

You will receive two medications: empagliflozin (Jardiance) 10 mg tablet and BI 690517 or placebo tablet

Both medications are taken orally (by mouth) once daily

One tablet is a film-coated tablet containing either BI 690517 or an inactive substance (placebo)

The other tablet contains empagliflozin, which all participants will receive

2 Monitoring kidney function

Your kidney function will be regularly measured through a value called eGFR (estimated glomerular filtration rate)

The first important measurement will be taken 3 months after starting the medication

Regular measurements will continue until your last scheduled visit

3 Long-term follow-up

The study will continue until July 2028

During this time, you will be monitored for:

Changes in kidney disease status

Any hospital stays related to heart failure

Overall cardiovascular health

4 Health monitoring

The medical team will track if your kidney function decreases by 40% or more from your starting point

Any hospital stays will be recorded, particularly those related to heart problems

Your overall heart health will be monitored throughout the study period

Who Can Join the Study?

  • You must be at least 18 years old at the time of screening
  • You must have evidence of chronic kidney disease that shows risk of progression, documented by laboratory tests from at least 3 months before screening and at the screening visit
  • You must meet one of these kidney function criteria:
    • Your kidney function test (eGFR) shows results between 20 and 45 units (mL/min/1.73m²), or
    • Your kidney function test (eGFR) shows results between 45 and 90 units (mL/min/1.73m²) with elevated protein levels in urine (uACR of at least 200 mg/g or protein-to-creatinine ratio of at least 300 mg/g)
  • Both men and women can participate in the study

Who Cannot Join the Study?

  • Age below 18 years
  • Severe allergic reactions to empagliflozin (a diabetes medication) or similar medications
  • Pregnancy or planning to become pregnant during the study period
  • Currently breastfeeding
  • Participation in another clinical trial within the past 30 days
  • History of serious kidney problems requiring dialysis
  • Uncontrolled diabetes mellitus (blood sugar disease)
  • Severe liver disease
  • Recent heart attack or stroke (within the last 3 months)
  • Active cancer or ongoing cancer treatment
  • History of organ transplantation
  • Severe uncontrolled high blood pressure
  • Serious infections that require hospitalization
  • Blood disorders that increase risk of bleeding
  • Unable to take medications by mouth
  • Mental conditions that could interfere with following study procedures
  • Alcohol or drug abuse within the past 6 months
  • Life expectancy less than 12 months due to other medical conditions

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Other Sites

Site Name City Country Status
Unidade Local De Saude De Sao Jose E.P.E. Lisbon Portugal
Klinikum der Technischen Universitaet Muenchen (TUM Klinikum) Munich Germany
Danderyds Sjukhus AB Danderyd Sweden
Azienda Ospedaliero-Universitaria Sant Andre Rome Italy
Casa Sollievo Della Sofferenza San Giovanni Rotondo Italy
Centre hospitalier universitaire de Liege Liege Belgium
Staedtisches Klinikum Braunschweig gGmbH Brunswick Germany
Herz Und Diabeteszentrum NRW Bad Oeynhausen Universitaetsklinik Der Ruhr-Universitaet Bochum Bad Oeynhausen Germany
Robert Bosch Krankenhaus GmbH Stuttgart Germany
Klinikum Dortmund gGmbH Dortmund Germany
Barmherzige Brueder Trier gGmbH Trier Germany
Universitaetsklinikum Aachen AöR Aachen Germany
Universitaetsklinikum Schleswig-Holstein AöR Kiel Germany
Azienda Unita Locale Socio Sanitaria N 8 Berica Vicenza Italy
Unidade Local De Saude De Loures-Odivelas EPE Loures Portugal
Fondazione IRCCS San Gerardo Dei Tintori Monza Italy
Unidade Local De Saude De Matosinhos E.P.E. Senhora Da Hora Portugal
Zentrum Fuer Nieren Hochdruck Und Stoffwechselerkrankungen Hanover Germany
HUmani Charleroi Belgium
Servico de Saude da Regiao Autonoma Da Madeira EPERAM Funchal Portugal
Steno Diabetes Center Copenhagen Herlev Denmark
Region Vaesternorrland Sundsvall Sweden
Ospedale Cardinal Massaia Asti Italy
Azienda Socio Sanitaria Territoriale Lariana Como Italy
Universita’ Degli Studi Di Perugia Perugia Italy
Region Skane Skanes Universitetssjukhus Lund Sweden
Azienda Ospedaliera di Padova Padua Italy
Sjællands Universitetshospital Roskilde Denmark
ClinPhenomics CVC GmbH Frankfurt Germany
Universitaetsklinikum Regensburg AöR Regensburg Germany
Fondazione IRCCS Ca Granda Ospedale Maggiore Policlinico Milan Italy
Ospedale San Raffaele S.r.l. Milan Italy
Universita’ Degli Studi Di Verona Verona Italy
Universitaetsklinikum Magdeburg AöR Magdeburg Germany
DKD HELIOS Klinik Wiesbaden GmbH Wiesbaden Germany
Karolinska University Hospital Solna Sweden
Lillebaelt Hospital Kolding Denmark
Az St-Jan Brugge-Oostende A.V. Brugge Belgium
Saarland University Hospital Homburg Germany
Westpfalz-Klinikum GmbH Kaiserslautern Germany
IRCCS Ospedale Policlinico San Martino Genoa Italy
Helios Universitaetsklinikum Wuppertal Wuppertal Germany
Aalborg University Hospital Aalborg Denmark
Rheinische Friedrich-Wilhelms-Universitaet Bonn Bonn Germany
Azienda Sociosanitaria Territoriale Santi Paolo E Carlo Milan Italy
Justus-Liebig-Universitaet Giessen Giessen Germany
Azienda USL Toscana Centro Prato Italy
Azienda Sanitaria Locale Citta Di Torino Turin Italy
Holbaek Sygehus Holbæk Denmark
Centro Hospitalar Do Baixo Vouga E.P.E. (CHBV E.P.E.) Aveiro Portugal
Centro Hospitalar de Setubal E.P.E. Setubal Portugal
ARNAS G. Brotzu Cagliari Italy
Azienda Sanitaria Locale 2 Lanciano Vasto Chieti Chieti Italy
Schwarzwald-Baar Klinikum Villingen-Schwenningen GmbH Villingen-Schwenningen Germany
Ziekenhuis Oost Limburg Genk Belgium
Rigshospitalet Copenhagen Denmark
Klinikum Konstanz GmbH Konstanz Germany
Fondazione Salvatore Maugeri Clinica Del Lavoro E Della Riabilitazione Pavia Italy
Vrije Universiteit Brussel Jette Belgium
Queen Silvia Childrens Hospital – Sahlgrenska University Hospital – Vaestra Goetalandsregionen Gothenburg Sweden
Multimedica S.p.A. Milan Italy
Odense University Hospital Odense Denmark
Agaplesion Frankfurter Diakonie Kliniken gGmbH Frankfurt Germany
Nierenzentrum Freiburg Freiburg Im Breisgau Germany
Dialysezentrum Neckersulm Neckarsulm Germany
Nephrologisches Zentrum Emsland Lingen (Ems) Germany
Cqabuubru Uelfdofrxgxckh Sfudsosnm Woluwe-Saint-Lambert Belgium
Udabwlm Lujls dc Snzpx dp Aauodwo Effbay Faro Portugal
Alokuyd Occkmqdihfb Uhoylezlhryva Pucgd Parma Italy
Uzxwasxjuy Mncxcgg Ctupqe Htqdticmmajifsoyo Hamburg Germany
Npxhqodxvhswzb Bng Bqv Kqhooftjy Bad Kreuznach Germany
Kum Nzpfujvbqlrwy Kqeafod Kronach Germany
Kza Kwpmtcujdj Fkgb Dthbwdw Uul Nypsrgyrpmtumqpucanhz ezwd Leipzig Germany
Kjtelpbpfxrqsacqd Tbzzkkvohm Traunstein Germany
Kugkadom Ntlqueoyi Cmxzdz Sli Nürnberg Germany
Mev Dcmoxxxsor unm Surzbykpeibcnxe Huavuexfkgk Gkcu Berlin Germany
Irpowopjrfrmoj Gzjzvajdbtmzibvzkxb uso Dqkmnkhnqrxudv Luvdbihv Landshut Germany
Riamyfuesbqwsvcci Gjmu Coburg Germany
Djrnqlfbgggmtl Hnwkwrvyv Heilbronn Germany
Denmptrxewrqff Efnvhuytp Elsenfeld Germany
Dhpshegepzwsbf Bstiwo Bremen Germany
Ajfxoaz Kfmvb Zenkfmm fatg Mgjckjn uok Rmlzopygguhqji ggupx Essen Germany
Mkp Dfteassbavysfv Shzmqakpivj Schweinfurt Germany
Nmhoswihrvhn Bhz Njthtqsr Bad Nenndorf Germany
Umbqmpqoapcaxkjvnacre i Loldinsqo Linkoping Sweden
Anmhsqs Uslro Sysalfgii Lpkthy Dd Idtbw Imola Italy
Avbycct Uomnq Llbnyf Snrht Sebiwyvbb Nw 1 Dffwkgtr Feltre Italy
Akochzs Snnbetnwj Lrwblm Dqf Vmesemp Cuyaa Odqqcx Verbania Italy
Sjkplapbsmdi Kfhgvvdw Snhqeqpf gyfhe Solingen Germany
Avy Tnu Chieri Italy
Arupwdq Svpdwtfzmklfib Lvlpkw 2 Savona Italy
Mzzzbf Hgzvljxe Hufcw Ueyjavktkawdwqvkkabc dkf Rvdohmfncvqsgdal Bduehl Herne Germany
Htpfdr Hbgmcnan Herlev Denmark
Uijhhzl Uwjgbphlop Huegczzy Uppsala Sweden
Ujbwjlyaigfgjxbxbqsxi Djizaxlbgkw Atl Duesseldorf Germany
Avuudby Ogbqfzptuye Nzjadbihy Sp Azpacdj E Bsykbv E C Aqrqah Ayabdcpqcko Alexandria Italy
Gzzrwu Ucvbmqsall Farifvbcm Frankfurt Germany
Kenwcdpx dql Uvumtonvrpow Myclncoz Agd Munich Germany
Ucltrmhjkfpbnazgpjjym Wwxydvtwo Ayt Wuerzburg Germany
Acphwzx Uideh Scnupwemk Ldyjhr Uxtwwi 1 Perugia Italy
Apaitih Uuhdu Sjxcfkdlt Lixbvm Dv Bqedlqr Bologna Italy
Aetthtb Odtigpumypd Pvlc Ggubapnm Xifzm Bergamo Italy
Mucsmgzkrpltxqjpvicrhjffao Hsfbyhzwgtxcytcv Halle (Saale) Germany
Hzrbtcfl Hfndzljd Hillerød Denmark
Uplwzeqopcmalgfxxren Riwmmhyejvpfllulqc Neuruppin 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 yet recruiting
01.07.2024
Denmark Denmark
Recruiting
01.07.2024
Germany Germany
Recruiting
01.07.2024
Italy Italy
Recruiting
01.07.2024
Portugal Portugal
Recruiting
01.07.2024
Sweden Sweden
Recruiting
01.07.2024

Trial locations

Investigated drugs:

BI 690517 is an aldosterone synthase inhibitor medication being tested to help prevent the worsening of kidney disease, reduce hospitalizations due to heart failure, and lower the risk of death from heart disease in people with kidney problems. This medication is taken as a daily pill.

Empagliflozin is a medication used to treat diabetes and heart failure. In this trial, it is being used in combination with BI 690517. It belongs to a class of medications called SGLT2 inhibitors, which work by helping the kidneys remove excess sugar from the blood through urine and can help protect both the heart and kidneys.

Investigated diseases:

Chronic kidney disease – A long-term condition where the kidneys gradually lose their ability to filter waste and excess fluid from the blood. The disease typically develops over many years as the tiny filters in the kidneys become damaged. This condition often progresses through several stages, from mild kidney damage to severe loss of kidney function. Common signs include changes in urination, swelling in legs and ankles, and fatigue. The disease can be associated with other health conditions such as high blood pressure and diabetes.

Heart failure – A chronic condition where the heart cannot pump blood effectively enough to meet the body’s needs. The heart muscle becomes weaker over time or has difficulty filling with blood. This leads to fluid buildup in the body, particularly in the lungs and extremities. Common symptoms include shortness of breath, fatigue, and swelling in the legs and ankles.

Cardiovascular disease – A group of conditions affecting the heart and blood vessels throughout the body. The disease typically develops when arteries become narrowed or blocked by fatty deposits. This process happens gradually over time and can affect blood flow to various parts of the body. The condition can involve multiple parts of the cardiovascular system and may progress differently in different people.

Trial ID:
2024-511025-63-00
Protocol code:
1378-0006
Trial Phase:
Therapeutic confirmatory (Phase III)

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