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Study to Evaluate the Effect of Balcinrenone/Dapagliflozin in Patients With Heart Failure and Impaired Kidney Function

RecruitingPhase 3

A Phase III, Randomised, Double-blind Study to Evaluate the Effect of Balcinrenone/Dapagliflozin, Compared With Dapagliflozin, on the Risk of Heart Failure Events and Cardiovascular Death in Patients With Heart Failure and Impaired Kidney Function

Who can join

Ages 18 to 130 · All sexes

Full eligibility criteria
Inclusion Criteria:

* Age ≥ 18 years
* Documented diagnosis of symptomatic HF (NYHA functional class II-IV)
* Having had a recent HF event within 6 months (hospitalization or urgent visit)
* Have a LVEF value from an assessment within the last 12 months
* Managed with SoC therapy for HF and renal impairment according to local guidelines
* NT-proBNP must be \>300 pg/mL (\>600 pg/mL if concomitant atrial fibrillation or atrial flutter)
* Not taking an MRA
* An eGFR ≥ 20 to \< 60 mL/min/1.73 m2
* Serum/plasma potassium ≤ 5.0 mmol/L

Exclusion Criteria:

* Acute coronary syndrome (unstable angina or myocardial infarction), stroke or transient ischaemic attack within the previous 3 months prior to enrolment or during the screening period
* Major cardiac surgery, coronary revascularisation or valvular repair or replacement, or implantation of a Cardiac resynchronisation therapy device within 3 months prior to enrolment or during the screening period, or planned to undergo any of these operations
* History of hypertrophic obstructive cardiomyopathy
* Complex congenital heart disease or severe uncorrected primary valvular disease
* Symptomatic bradycardia or second- or third-degree heart block without a pacemaker
* Systolic BP \< 90 mmHg, or symptomatic hypotension within the past 24 hours
* Primary pulmonary hypertension, chronic pulmonary embolism, severe pulmonary disease including COPD or exacerbation of COPD requiring invasive mechanical ventilation assistance within 12 months prior to enrolment
* Type 1 diabetes mellitus
* Kidney replacement therapy in the past 4 weeks, currently requiring kidney replacement or imminent plan to start kidney replacement therapy
* Acute or chronic liver disease with severe impairment of liver function, eg, ascites, oesophageal varices, coagulopathy, and encephalopathy
* Suspected or confirmed COVID-19 infection within the last 4 weeks or hospitalisation for COVID-19 within the last 12 weeks
* Treatment with strong or moderate CYP3A4 inhibitor or inducer

About the study

This is a Phase III, international, multi-centre, randomised, double-blind, parallel-group, double-dummy, active-controlled, event-driven study in patients with chronic HF and impaired kidney function who had a recent HF event. The aim is to evaluate the effect of balcinrenone/dapagliflozin vs dapagliflozin, given once daily on top of other classes of SoC, on CV death and HF events.

What is being tested

Sponsor: AstraZeneca · Participants: 3,850 · Started: Apr 12, 2024

Contact the study team

Official record on ClinicalTrials.gov — NCT06307652

Locations in the U.S.

AlabamaResearch Site, Alexander City
Research Site, Fairhope
Research Site, Huntsville
ArizonaResearch Site, Phoenix
Research Site, Phoenix
ArkansasResearch Site, Little Rock
CaliforniaResearch Site, Beverly Hills
Research Site, Covina
Research Site, Los Angeles
Research Site, Los Angeles
Research Site, Redding
Research Site, San Diego
Research Site, San Francisco
Research Site, Vista
Research Site, West Hills
ColoradoResearch Site, Aurora
FloridaResearch Site, Boca Raton
Research Site, Bradenton
Research Site, Delray Beach
Research Site, Fort Lauderdale
Research Site, Gainesville
Research Site, Jacksonville
Research Site, Miami
Research Site, Miami Lakes
Research Site, Palm Beach Gardens
Research Site, Pensacola
Research Site, Safety Harbor
Research Site, Saint Augustine
Research Site, St. Petersburg
Research Site, Tampa
GeorgiaResearch Site, Atlanta
Research Site, Atlanta
Research Site, Peachtree City
Research Site, Tucker
IllinoisResearch Site, Chicago
Research Site, Hazel Crest
Research Site, Peoria
Research Site, Winfield
IndianaResearch Site, Elkhart
Research Site, Evansville
Research Site, Hammond
Research Site, Muncie
Research Site, Munster
IowaResearch Site, Waterloo
KansasResearch Site, Wichita
LouisianaResearch Site, West Monroe
MarylandResearch Site, Rockville
MassachusettsResearch Site, Boston
Research Site, Worcester
MichiganResearch Site, Bloomfield Hills
Research Site, Ypsilanti
MinnesotaResearch Site, Saint Paul
MississippiResearch Site, Jackson
MissouriResearch Site, Columbia
Research Site, Kansas City
Research Site, Kansas City
NebraskaResearch Site, Lincoln
Research Site, Lincoln
NevadaResearch Site, Henderson
New JerseyResearch Site, Jersey City
Research Site, Somerset
New YorkResearch Site, Brooklyn
Research Site, Brooklyn
Research Site, Clifton Park
Research Site, New York
Research Site, Staten Island
Research Site, The Bronx
North CarolinaResearch Site, Asheville
Research Site, Chapel Hill
Research Site, Charlotte
Research Site, Durham
Research Site, Pinehurst
Research Site, Wilmington
OhioResearch Site, Cincinnati
Research Site, Cincinnati
Research Site, Springfield
OregonResearch Site, Portland
PennsylvaniaResearch Site, Abington
Research Site, Camp Hill
Research Site, Hershey
Research Site, Philadelphia
Rhode IslandResearch Site, Providence
South CarolinaResearch Site, Charleston
Research Site, Charleston
Research Site, Lancaster
South DakotaResearch Site, Rapid City
TennesseeResearch Site, Jackson
Research Site, Knoxville
Research Site, Memphis
Research Site, Nashville
Research Site, Tullahoma
TexasResearch Site, Allen
Research Site, Amarillo
Research Site, Amarillo
Research Site, Cypress
Research Site, Dallas
Research Site, Dallas
Research Site, Dallas
Research Site, El Paso
Research Site, Houston
Research Site, McKinney
Research Site, McKinney
Research Site, Odessa
Research Site, San Antonio
Research Site, Temple
Research Site, Tyler
Research Site, Tyler
UtahResearch Site, Salt Lake City
VirginiaResearch Site, Falls Church
Research Site, Newport News

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.