Study to Evaluate the Efficacy and Safety of AZD4831 in Participants With Heart Failure With Left Ventricular Ejection Fraction > 40%

Completed · Phase 2/Phase 3 · Has a placebo group

Conditions studied: Heart Failure With Preserved Ejection Fraction

In brief

This is a randomised, double-blind, placebo-controlled, multi-center sequential phase 2b and Phase 3 study to evaluate the efficacy and safety of AZD4831 administered for up to 48 Weeks in participants with heart failure with left ventricular ejection fraction \> 40%. The study will consist of 2 separate parts, Part A and Part B, approximately 660 participants will be randomised in Part A, 820 in Part B.

Key facts

Study ID

NCT04986202

Run by

AstraZeneca

People needed

711

Starts

2021-06-30

Expected to finish

2024-03-27

Last updated by the study team

2025-08-27

Who can join

Age: 40 and older, up to 85. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Part A
• ≥ 40 to ≤ 85 years of age, at the time of signing the informed consent.
• Documented stable symptomatic HF (New York Heart Association Class II-IV) for at least 1 month at Screening (Visit 1) (transient HF in the setting of an MI does not qualify), with a medical history of typical symptoms of HF and receiving optimal therapy for HF as determined by the health-care physician.
• LVEF > 40% at Screening (Visit 1). All participants will undergo a local echocardiogram at the Screening (Visit 1) with central reading to confirm the LVEF > 40% eligibility criteria before randomisation.
• 6MWD ≥ 30 meters and ≤ 400 meters at Screening (Visit 1) and Randomisation (Visit 3). Difference in 6MWD between Screening and Randomisation must be < 50 meters.
• KCCQ-TSS ≤ 90 points at Screening (Visit 1) and Randomisation (Visit 3)
• NT-proBNP ≥ 250 pg/mL (sinus rhythm) or ≥ 500 pg/mL (atrial fibrillation/flutter) at Screening (Visit 1) for patients with BMI ≤30 kg/m2.
• NT-proBNP ≥ 200 pg/mL (sinus rhythm) or ≥ 400 pg/mL (atrial fibrillation/flutter) at Screening (Visit 1) for patients with BMI > 30 kg/m2.
• The ECG performed at Screening should be used for heart rhythm evaluation.
• At least one of the following:
• Structural heart disease, ie, LA enlargement and/or left ventricular hypertrophy at the echocardiogram performed at Screening (Visit 1). Left atrial enlargement is defined by at least 1 of the following: LA width (diameter) ≥ 3.8 cm or LA length ≥ 5.0 cm, or LA area ≥ 20 cm2 or LA volume ≥ 55 mL or LAVI > 34 mL/m2. Left ventricular hypertrophy is defined by septal thickness or posterior wall thickness ≥ 1.1 cm or LVMI > 95 g/m2 in women and > 115 g/m2 in men.
• Spectral tissue Doppler echocardiography - E/e' ratio (average of septal and lateral) ≥ 13 at rest at the echocardiogram performed at Screening (Visit 1).
• Indirectly estimated elevation of PASP by TRmax velocity > 2.8 m/s (280 cm/s) (PASP > 35 mmHg) at the echocardiogram performed at Screening (Visit 1) OR directly measured pulmonary capillary wedge pressure > 15 mmHg at rest within the past 12 months or > 25 mmHg at exercise documented by right heart catheterisation within 12 months prior to Screening (Visit 1).
• HF decompensation within 6 months before Randomisation (Visit 3), defined as hospitalisation for HF or IV diuretic treatment for HF during an urgent, unscheduled visit without hospitalisation.
• Body mass index ≥ 18.0 kg/m2 and ≤ 45.0 kg/m2
• Male or female of non-childbearing potential.
• Part B
• Participant must be ≥ 40 to ≤ 85 years of age, at the time of signing the informed consent.
• Documented diagnosis of symptomatic HF (NYHA class II-IV) at Screening (Visit 1), and a medical history of typical symptoms/signs of heart failure ≥ 6 weeks before Screening (Visit 1), and receiving optimal therapy for HF as determined by the health-care physician, with at least intermittent need for diuretic treatment.
• LVEF >40% and evidence of structural heart disease (ie, left ventricular hypertrophy or
• left atrial enlargement [defined by at least one of the following:LA enlargement and/or left ventricular hypertrophy at the echocardiogram
• performed at Screening (Visit 1). Left atrial enlargement is defined by at least 1 of the following: LA width
• (diameter) ≥ 3.8 cm or LA length ≥ 5.0 cm, or LA area ≥ 20 cm2 or LA volume ≥ 55 mL or LAVI > 34
• mL/m2. Left ventricular hypertrophy is defined by septal thickness or posterior wall thickness ≥ 1.1 cm or
• LVMI > 95 g/m2 in women and > 115 g/m2 in men.]) documented by the most recent echocardiogram, or cardiac

You may not qualify if…

• Part A
• 1 eGFR < 30 mL/min/1.73m2 (Chronic Kidney Disease-Epidemiology Collaboration formula) at Screening (Visit 1).
• Systolic blood pressure < 90 mmHg or ≥ 160 mmHg if not on treatment with ≥ 3 blood pressure lowering medications or ≥ 180 mmHg irrespective of treatments at Randomisation
• Heart rate > 110 bpm or < 50 bpm at Randomisation
• Life expectancy < 3 years due to other reasons than cardiovascular disease.
• History or ongoing allergy/hypersensitivity reactions to drugs (including but not limited to rash, angioedema, acute urticaria).
• Presence of any disease or condition rather than HF constituting the main reason for limiting the ability to exercise/reduced exercise capacity.
• Current decompensated HF and/or NT-proBNP > 5000 pg/mL at Screening (Visit 1)
• Documented history of ejection fraction ≤ 40%.i.e. HF with recovered ejection fraction. Transient ejection fraction decrease e.g. in the setting of an MI does not apply
• Any planned cardiovascular procedure (eg, coronary revascularisation, ablation of atrial fibrillation/flutter, valve repair/replacement, aortic aneurysm surgery, etc).
• Any cardiac event (eg, myocardial infarction, unstable angina), coronary revascularisation (percutaneous coronary intervention or coronary artery bypass grafting), ablation of atrial fibrillation/flutter, valve repair/replacement, implantation of a cardiac resynchronisation therapy device within 12 weeks prior to Screening (Visit 1) or between Screening and Randomisation. Patients who underwent a successful atrial fibrillation/flutter cardioversion, can be enrolled in the study after 4 weeks.
• Hb < 110 g/L (male) and < 100 g/L (female) or iron-deficiency with/without anaemia requiring ongoing or planned IV iron treatment.
• Participants with hyperthyroidism, uncontrolled hypothyroidism (including but not limited to TSH ≥10 mIU/mL), or any clinically significant thyroid disease as judged by the investigator.
• ALT or AST ≥ 2 × ULN at Screening (Visit 1).
• Pulmonary arterial hypertension, chronic pulmonary embolism, severe pulmonary disease including COPD (ie, requiring home oxygen, chronic nebulizer therapy or chronic oral steroid therapy, or hospitalization for exacerbation of COPD requiring ventilatory support within 12 months prior to Screening (Visit 1).
• Any active infection requiring oral, intravenous or intramuscular treatment at Screening (Visit 1) and/or at Randomisation.
• 23 Any signs or confirmation of COVID-19 infection:
• Suspected (as judged by PI) or confirmed COVID-19 within the last 2 weeks prior to Screening (Visit 1) or at Randomisation.
• Hospitalisation for COVID-19 within the last 12 weeks prior to Screening (Visit 1).
• Any concomitant medications known to be a potent CYP3A4 inducers or inhibitors, eg, itraconazole, rifampicin, clarithromycin, or propylthiouracil
• Previous enrolment and randomisation in the present study. (Participants who where screened and screen failed and not randomised in Part A can be screened for possible entry to Part B).
• All exclusion criteria in Part A are applicable to Part B with the following exceptions:
• Exclusion criteria 4; 19
• Exclusion Criteria specific for Part B only [criteria numeration for Part B]
• Life expectancy < 2 years due to other reasons than cardiovascular disease.

Where it is running

• Research Site — Little Rock, Arkansas, United States
• Research Site — Sacramento, California, United States
• Research Site — Miami, Florida, United States
• Research Site — Miami Beach, Florida, United States
• Research Site — Ocala, Florida, United States
• Research Site — Evanston, Illinois, United States
• Research Site — Hazel Crest, Illinois, United States
• Research Site — Shreveport, Louisiana, United States
• Research Site — Baltimore, Maryland, United States
• Research Site — St Louis, Missouri, United States
• Research Site — Buffalo, New York, United States
• Research Site — New York, New York, United States
• Research Site — Rosedale, New York, United States
• Research Site — Chapel Hill, North Carolina, United States
• Research Site — Pinehurst, North Carolina, United States
• Research Site — Cleveland, Ohio, United States
• Research Site — Philadelphia, Pennsylvania, United States
• Research Site — Knoxville, Tennessee, United States
• Research Site — Tullahoma, Tennessee, United States
• Research Site — Norfolk, Virginia, United States
• Research Site — Bedford Park, Australia
• Research Site — Chermside, Australia
• Research Site — Concord, Australia
• Research Site — Frankston, Australia
• Research Site — Alexander City, Alabama, United States

Full record on ClinicalTrials.gov

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