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Trial · Interventional

CompletedPhase 4Registry data

Cardiac and Metabolic Effects of Semaglutide in Heart Failure With Preserved Ejection Fraction

Overview

Status
Completed
Phase
Phase 4
Enrollment
81 participants (actual)
Sponsor
Mayo Clinic · Other
Design
Randomized · Double masking
Countries
1 country

United States

Start
6 Sept 2022
Primary completion
17 Jul 2026
Completion
17 Jul 2026
First posted
12 May 2022
Last update posted
14 Aug 2026
Conditions
Cardiomyopathy · Heart Failure With Preserved Ejection Fraction (HFpEF) · Obesity

Timeline

1 trial · 1 completed

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
202220232024202520262027
  1. Ph 4

    Cardiac and Metabolic Effects of Semaglutide in Heart Failure With Preserved Ejection Fraction

    NCT05371496

    6 Sept 2022 to 17 Jul 2026

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

The purpose of this research is to find out if an aggressive intervention to lose weight, will improve symptoms in patients with obesity-related cardiomyopathy, which is also known as the obese phenotype of heart failure with preserved ejection fraction (HFpEF).

Interventions

  • SemaglutideDrug
  • PlaceboDrug
  • Counselling on healthy lifestyle interventionBehavioral

Arms2

  • Active comparator

    Semaglutide Treatment

    Subjects will receive Semaglutide once weekly in addition to counselling on healthy lifestyle intervention

  • Placebo comparator

    Placebo Treatment

    Subjects will receive matching placebo once weekly in addition to counselling on healthy lifestyle intervention

Primary outcomes1

Outcomes the sponsor listed as primary.

  1. Pulmonary Capillary Wedge Pressure (PCWP)

    Time frame · Baseline, 12 months

    Registry description

    Change in PCWP during exercise, reported in mmHG

Secondary outcomes(20)
  1. Trans-cardiac uptake of free fatty acids (FFA) at rest

    Time frame · Baseline, 12 months

    Registry description

    Change in trans-cardiac uptake of FFA will be measured using arterial and coronary sinus blood samples collected at rest during cardiac catheterization procedure.

  2. Trans-cardiac uptake of free fatty acids (FFA) during exercise

    Time frame · Baseline, 12 months

    Registry description

    Change in trans-cardiac uptake of FFA will be measured using arterial and coronary sinus blood samples collected during the exercise portion of the cardiac catheterization procedure.

  3. Trans-cardiac uptake of glucose at rest

    Time frame · Baseline, 12 months

    Registry description

    Change in trans-cardiac uptake of glucose will be measured using arterial and coronary sinus blood samples collected at rest during the cardiac catheterization procedure.

  4. Trans-cardiac uptake of glucose during exercise

    Time frame · Baseline, 12 months

    Registry description

    Change in trans-cardiac uptake of glucose will be measured using arterial and coronary sinus blood samples collected during the exercise portion of the cardiac catheterization procedure.

  5. Trans-cardiac uptake of ketone bodies at rest

    Time frame · Baseline, 12 months

    Registry description

    Change in trans-cardiac uptake of ketone bodies will be measured using arterial and coronary sinus blood samples collected at rest during the cardiac catheterization procedure.

  6. Trans-cardiac uptake of ketone bodies during exercise

    Time frame · Baseline, 12 months

    Registry description

    Change in trans-cardiac uptake of ketone bodies will be measured using arterial and coronary sinus blood samples collected during the exercise portion of the cardiac catheterization procedure.

  7. Left ventricular (LV) global longitudinal strain

    Time frame · Baseline, 12 months

    Registry description

    Change in LV global longitudinal strain will be assessed by echocardiography conducted during the cardiac catheterization procedure

  8. Left Atrial (LA) reservoir strain

    Time frame · Baseline, 12 months

    Registry description

    Change in LA reservoir strain will be assessed by echocardiography conducted during the cardiac catheterization procedure

  9. Right Ventricular (RV) free wall strain

    Time frame · Baseline, 12 months

    Registry description

    Change in RV free wall strain will be assessed by echocardiography conducted during the cardiac catheterization procedure

  10. Myocardial mass

    Time frame · Baseline, 12 months

    Registry description

    Change in myocardial mass will be measured by CMR imaging.

  11. Myocardial volume

    Time frame · Baseline, 12 months

    Registry description

    Change in myocardial volume will be measured by CMR imaging.

  12. Myocardial fat content

    Time frame · Baseline, 12 months

    Registry description

    Change in myocardial fat content will be measured by CMR imaging.

  13. Body fat mass

    Time frame · Baseline, 12 months

    Registry description

    Change in body fat mass will be measured using dual X-ray absorptiometry (DEXA)

  14. Visceral fat content

    Time frame · Baseline, 12 months

    Registry description

    Change in visceral fat content will be measured using limited abdominal MRI

  15. Total blood volume

    Time frame · Baseline, 12 months

    Registry description

    Change in total blood volume will be assessed by using the radiolabeled iodinated albumin (131I, 5-25 μCu) indicator dilution technique (BVA-100 Blood Volume Analyzer, Daxor Corp, NY).

  16. Total plasma volume

    Time frame · Baseline, 12 months

    Registry description

    Change in total plasma volume will be assessed by using the radiolabeled iodinated albumin (131I, 5-25 μCu) indicator dilution technique (BVA-100 Blood Volume Analyzer, Daxor Corp, NY).

  17. Change in Quality of Life (QOL) as assessed by Kansas City Cardiomyopathy Questionnaire (KCCQ)

    Time frame · Baseline, 12 months

    Registry description

    KCCQ was a 23-item, self-administered questionnaire that measure the participant's perception of their health status, including their heart failure (HF) symptoms, impact on physical and social function and how their HF impacts the quality of life. KCCQ quantifies 7 domains: physical limitations (6 items), symptom stability (1 item), symptom frequency (4 items), symptom burden (3 items), self-efficacy (2 items), quality of life (3 items) and social limitations (4 items). Scores were generated for each domain and scaled from 0 to 100, with 0 (worst) and 100 (the best possible status), where the higher score reflected better health status.

  18. Change in skeletal muscle mass

    Time frame · Baseline, 12 months

    Registry description

    Change in skeletal muscle mass will be determined using DEXA scan

  19. Change in cardiac chamber mass

    Time frame · Baseline, 12 months

    Registry description

    Change in cardiac chamber mass and volumes will be measured by CMR imaging

  20. Proportion of patients that no longer fulfill hemodynamic criteria for HFpEF at end of trial

    Time frame · 12 months

    Registry description

    Proportion of patients that no longer fulfill hemodynamic criteria for HFpEF at end of trial, defined as resting PAWP\<15 and exercise PAWP\<25

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

No results are posted for this trial.

Completed trials do not always post results.

Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works

Studies0

Studies that cite this trial.

No study cites this trial.

Eligibility

Who could join, as posted.

Sex
All
Age
from 18 Years
Healthy volunteers
Not accepted
Inclusion and exclusion criteria, as posted
Inclusion Criteria: * BMI ≥ 30.0 kg/m2. * NYHA Class II-IV. * LVEF ≥ 50 % within the preceding year. * No hospitalizations due to heart failure in the preceding 30 days. * At least one of the following: 1. Mean PCWP ≥ 15 mmHg or left ventricular end diastolic pressure (LVEDP) ≥ 15 mmHg documented during catheterization at rest, or PCWP or LVEDP ≥ 25 mmHg documented during catheterization at exercise. 2. If BMI \< 35.0: NT-proBNP ≥ 220 pg/mL (for patients with sinus rhythm) or NT-proBNP ≥ 660 pg/mL (for patients with persistent/permanent atrial fibrillation); if BMI ≥ 35.0: NT-proBNP ≥ 125 pg/mL (for patients in sinus rhythm) or NT-proBNP ≥ 375 pg/mL (for patients with persistent/ permanent atrial fibrillation) at screening (NT-proBNP analyzed by the central laboratory) in combination with at least one of the following (documented by echocardiography within 12 months prior to or at screening): i. Septal é \< 7 cm/sec or lateral é \< 10 cm/sec or average E/é ≥ 15. ii. PA systolic pressure \> 35 mmHg. iii. Left atrial (LA) enlargement (LA width ≥ 3.8 cm or LA length ≥ 5.0 cm or LA area ≥ 20.0 cm2 or LA volume ≥ 55 mL or LA volume index ≥ 29 mL/m2). iv. LV hypertrophy with septal thickness or posterior wall thickness ≥ 1.2 cm 3. Hospitalization with a primary diagnosis of decompensated heart failure which required intravenous (IV) loop diuretic treatment, within the previous 12 months in combination with at least two of the following (documented by echocardiography within 12 months prior to or at screening): i. Septal é \< 7 cm/sec or lateral é \< 10 cm/sec or average E/é ≥ 15. ii. PA systolic pressure \> 35 mmHg. iii. LA enlargement (LA width ≥ 3.8 cm or LA length ≥ 5.0 cm or LA area ≥ 20.0 cm2 or LA volume ≥ 55 mL or LA volume index ≥ 29 mL/m2). iv. LV hypertrophy with septal thickness or posterior wall thickness ≥ 1.2 cm. v. Ongoing use of diuretic therapy for at least 30 days prior to screening. Exclusion Criteria: Cardiovascular-related: * Myocardial infarction, stroke, hospitalization for heart failure, unstable angina pectoris or transient ischemic attack within 30 days prior to the day of screening. * Systolic blood pressure \> 160 mmHg at screening. * Planned coronary, carotid or peripheral artery revascularization. * Any other condition judged by the investigator to be the primary cause of dyspnea (such as heart failure due to restrictive cardiomyopathy or infiltrative conditions (e.g., amyloidosis), hypertrophic obstructive cardiomyopathy, primary pulmonary arterial hypertension, chronic obstructive pulmonary disease, right heart failure due to pulmonary disease, complex congenital heart disease, anemia, or more than moderate mitral or aortic heart valve disease). * Amyloid cardiomyopathy may be present in 5-15% of patients presenting with the clinical syndrome of HFpEF,60-62 and patients with amyloid may respond differently to WL intervention. To enhance the scientific rigor of the trial by ensuring a homogenous population of true primary HFpEF, we will carefully evaluate for the presence of amyloid using the approach outlined in a recent scientific statement from the AHA,63 which is also consistent with our current clinical practice. * Specifically, potential participants will be evaluated for clues or risk factors for underlying cardiac amyloid including intolerance to antihypertensives, hypotension, orthostatic intolerance, persistent low-grade elevation in troponin, low QRS voltage on ECG, unexplained AV block or prior pacemaker, unexplained LV or RV wall thickening, impaired LV global longitudinal strain with apical sparing by echocardiography, family history of cardiomyopathy, neuropathy, autonomic dysfunction, carpal tunnel syndrome, lumbar spinal stenosis, family history of polyneuropathy, or black race. Patients with these risk factors will undergo screening evaluation for amyloid prior to consent in CAMEO-SEMA as part of best clinical practice. This includes screening for monoclonal light chain as first step, followed by hematology consultation if the screen is positive. Patients with risk factors but no monoclonal light chain will then undergo Tc-99m-PYP scan to rule out cardiac amyloid. Obesity-related: * Bariatric surgery prior to screening within 5 years of screening or planned bariatric surgery within the trial time course. * A self-reported change in body weight \> 5 kg (11 lbs) within 90 days before screening irrespective of medical records. Glycemia-related: * HbA1c ≥ 10.0% based on latest available value from medical records, not older than 3 months * History of type 1 diabetes (history of gestational diabetes is allowed). * Treatment with any GLP-1 receptor agonist within 90 days prior to the day of screening. General health and safety: * Personal or first-degree relative(s) history of multiple endocrine neoplasia type 2 or medullary thyroid carcinoma. * Presence of acute pancreatitis within the last 180 days prior to screening. * History or presence of chronic pancreatitis. * End-stage renal disease or chronic or intermittent hemodialysis or peritoneal dialysis. * Presence or history of malignant neoplasm within 5 years prior to the day of screening. Basal and squamous cell cancer and any carcinoma in-situ are allowed. * Known or suspected hypersensitivity to trial product(s) or related products. * Participation in any clinical trial of an approved or non-approved device for the treatment of heart failure or obesity within 30 days before screening. * Receipt of any investigational medicinal product within 30 days before screening. * Female who is pregnant, breast-feeding or intends to become pregnant or is of child-bearing potential and not using a highly effective contraceptive method. * Major surgery scheduled for the duration of the trial, affecting walking ability in the opinion of the investigator. * Any disorder, including severe psychiatric disorder, suicidal behavior within 90 days before screening, and suspected drug abuse, which in the investigator´s opinion might jeopardize subject´s safety or compliance with the protocol.

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