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Heart Failure With Reduced Ejection FractionNCT05795400

Administration of the SGLT-2 Inhibitor Dapagliflozin in the Patients With Amyloid Cardiomyopathy

A study testing Dapagliflozin 10mg Tab in people with Heart Failure With Reduced Ejection Fraction and Heart Failure With Preserved Ejection Fraction, run by National Medical Research Center for Cardiology, Ministry of Health of Russian Federation at 1 site in Russia.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record

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Trial summary

Efficacy and safety of early administration of the SGLT-2 inhibitor dapagliflozin will be evaluated in patients with HF, regardless of LVEF, due to amyloid cardiomyopathy. Read more about this study

Who is it for?
Ages 18 to 80 years
What is being tested?
Dapagliflozin 10mg Tab
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
50 participants
Where
1 siteRussia
Study dates
1 Jun 2022to 30 Sep 2025
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Males and females between 18 and 80 years of age
  • HF, confirmed with the increased level of NT-proBNP>300 pg/mL or BNP>100 pg/mL
  • Transthyretin amyloid cardiomyopathy, confirmed with echocardiography and/or contrast-enhanced cardiac MRI

Who cannot join

  • The inability to continue all the activities planned in this study by the patient.
  • The onset of pregnancy.
  • Patient's voluntary withdrawal of consent to participate in a clinical trial at any point during the conduct of the study.
  • Development of intolerable side effects.
  • Administration of disease-modifying treatment of amyloidosis.

Trial locations and contacts

1 site in 1 country.

Russia1 site
  • National Medical Research Center for Cardiology, Ministry of Health of Russian Federation

    Moscow, 121552

Other trials in Russia

About this study

Official title: Administration of the SGLT-2 Inhibitor Dapagliflozin in the Patients With Amyloid Cardiomyopathy: a Pilot Study

Efficacy and safety of early administration of the SGLT-2 inhibitor dapagliflozin will be evaluated in patients with HF, regardless of LVEF, due to amyloid cardiomyopathy.

Read the detailed description

Amyloidosis is an infiltrative disease in which fibrillar glycoprotein amyloid is deposited in the tissues. The prevalence of amyloidosis remains largely unexplored, but if the wild type of transthyretin amyloidosis is considered, it still remains significantly underestimated in the population. Among patients hospitalized for heart failure with a preserved left ventricular ejection fraction (HFpEF), 13% are later diagnosed with amyloid cardiomyopathy (AC), in 20-25% of patients over 80 years old AC is a finding of pathologists, and in the oldest group of patients over 97 years old AC is identified in 37% of cases. Hereditary transthyretin amyloidosis occurs at less than 8.8 cases per 1 million population in non-endemic areas (e.g., Sicily) and 1 case per 1000 population in endemic areas (e.g., Portugal). Thus, the prevalence of amyloid cardiomyopathy as the cause of HFpEF is underestimated.

One of the manifestations of systemic amyloidosis is amyloid cardiomyopathy, when amyloid is deposited in the myocardium. This leads to thickening walls (phenotype of hypertrophic cardiomyopathy) and impaired relaxation processes, leading to diastolic myocardial dysfunction up to restrictive disorders (restrictive cardiomyopathy phenotype). Thus, in patients with amyloid cardiomyopathy HFpEF develops, and with the progression of the disease - heart failure with the mildly reduced (HFmrEF) and reduced (HFrEF) ejection fraction. The tragedy of situation lies in the fact that the specific (disease-modifying) treatment aimed at stopping or delaying amyloid deposition is limited to only two types of amyloidosis: AL and ATTR. As for the symptomatic treatment of HF, unfortunately, according to specific changes in hemodynamics, even with the reduced LVEF, therapy with beta-blockers, ACE-I/ARB/ARNI should be canceled. Currently, with the manifestation of the symptoms of HF, strict control over the drinking regimen and hydrobalance is necessary, and salt intake should be limited. In case of oedema, treatment with loop diuretics, MRA should be administrated. To date, in the treatment of HF, both with the reduced and preserved LVEF, another group of drugs has appeared - sodium-glucose cotransporter-2 (SGLT-2) inhibitors. However, in all studies conducted, the presence of HCM/RCM was the non-inclusion criteria in the investigation. At the same time, this group of drugs, unlike beta-blockers/ACE-I/ARNI, doesn't have such a significant effect on central hemodynamics, but it can have a positive antiproliferative, metabolic and nephroprotective effect.

Thereby, the study of SGLT-2 use in patients with amyloid cardiomyopathy with any phenotype of HF compared to placebo is of special interest.

Aims: Determination of the possibility of influence of early administration of SGLT-2 inhibitor dapagliflozin on a course of the disease (functional status, clinical and laboratory parameters, systolic and diastolic function of the left and right ventricular, cardiac strain parameters, parameters of target organ functions) in patients with the acute decompensated heart failure (ADHF), regardless of LVEF, against the background of transthyretin amyloid cardiomyopathy.

Being tested
Dapagliflozin 10mg Tab, Placebo
Keywords
heart failure, amyloidosis, cardiomyopathy, amyloid cardiomyopathy
Medical subject headings
Amyloid Neuropathies, Familial, Heart Failure, Amyloidosis, Cardiomyopathies

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Dapagliflozin 10mg TabDrug

    10 mg tablets given once daily, per oral use

  • PlaceboDrug

    tablet of placebo drug dosed once daily

Study groups in NCT05795400
Study groupRoleWhat they receive
Dapagliflozine groupExperimental20 patients diagnosed with heart failure and amyloid cardiomyopathy, regardless of HF phenotype, are planned to be enrolled in the study. Patients with the edematous syndrome are allowed to participate in the study, but the condition of stable hemodynamics must be observed. Regardless of the group, patients will receive standard therapy for ADHF (diuretics and MRA). Patients will not receive beta-blockers/ACE-I/ARNI. In the treatment group the therapy will include the SGLT-2 inhibitor dapagliflozin, which will be prescribed during the first 24 hours after the hospitalization.
Receives: Drug: Dapagliflozin 10mg Tab
Control groupPlacebo comparatorIn the control group, patients will be treated with standard diuretic therapy without SGLT-2 inhibitors.
Receives: Drug: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Effect of dapagliflozin on quality of life using Kansas City Cardiomyopathy Questionnaire Summary Score (KCCQ-SC)

    Changes in KCCQ score will be assessed

    Measured: 6 months

  2. Effect of Dapagliflozin on 6 Minute Walk Test Distance

    Changes in 6MWT score will be assessed

    Measured: 6 months

  3. Effect of dapagliflozin on N-terminal Pro B-type Natriuretic Peptide (NTproBNP)

    Changes in concentration of NT-proBNP will be assessed

    Measured: 6 months

Secondary outcomes (3)
  1. Cardiovascular death + number of hospitalizations due to heart failure

    Measured: 6 months

  2. Effect of dapagliflozin on change in echocardiographic parameters

    Left ventricular ejection fraction will be assessed

    Measured: 6 months

  3. Effect of dapagliflozin on change in specle-tracking echocardiographic parameters

    Global longitudinal strain will be assessed

    Measured: 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Apr 2023
  2. Study start1 Jun 2022
  3. Primary completion30 May 2025
  4. Study completion30 Sep 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
a single-center, pilot, prospective, randomized, placebo-controlled clinical trial
Masking
Single blind
Who is masked
Participant
Enrolment
50 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05795400
Sponsor's protocol ID
20230120
Status last verified
Apr 2026
First submitted
20 Jan 2023
Last updated
24 Apr 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

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