Maridebart Cafraglutide for Heart Failure and Obesity in Adults
Tests maridebart cafraglutide in adults with heart failure and obesity against placebo.
Plain-language title generated from the registry record
Registry title: Maridebart Cafraglutide in Heart Failure With Preserved or Mildly Reduced Ejection Fraction and Obesity (MARITIME-HF)
Key facts
- Where
- Bari, Bergamo, Brescia, Cortona, Foggia, Forli', Milan, Naples, Parma, Pavia, Rimini, Rivoli, Rome, Rozzano, and Sassari, ItalySee the 17 sites
- Phase
- Phase 3
AI summary: who the study is looking for
From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
The trial is looking for adults with heart failure and obesity (BMI 30 or higher) whose heart pumps with an ejection fraction above 40%. It tests maridebart cafraglutide against placebo.
- Age
- 18 years or older (or the legal age in the country, if that is older than 18).
- Sex
- All sexes can join.
- Disease stage
- Heart failure diagnosed at least 30 days ago, NYHA Class II-IV, with a documented LVEF above 40% in the last 12 months. BMI 30 kg/m2 or higher.
- Earlier treatment
- Must be on standard heart failure treatment, stable for at least 14 days before randomization. If they have type 2 diabetes, treatment must be stable for at least 14 days. Cannot have used GLP-1 RA, GIP agonists or antagonists, amylin analogs or weight-loss medicines in the 90 days before or during screening.
- Biomarker or test result
- Documented LVEF above 40%. Calcitonin must be below 50 ng/L (pg/mL) at screening.
Main reasons for not taking part
- Heart attack, valve surgery, bypass or other major heart surgery, or stroke in the last 60 days
- Type 1 diabetes, or HbA1c above 10.0% (86 mmol/mol) in people with type 2 diabetes
- Personal or close family history of medullary thyroid carcinoma or MEN-2
- Heart failure caused by conditions such as hypertrophic cardiomyopathy, amyloid, myocarditis or constrictive pericarditis
- eGFR below 20 mL/min/1.73 m2 or on dialysis
Read by machine on 12 November 2026.
Where in Italy
- Azienda Universitaria Ospedaliera Consorziale Policlinico BariBari, ItalyTaking people
- Azienda Socio Sanitaria Territoriale Papa Giovanni XXIIIBergamo, ItalyTaking people
- Azienda Socio Sanitaria Territoriale degli Spedali Civili di BresciaBrescia, ItalyTaking people
- Azienda Unita' Sanitaria Locale Toscana Sud EstCortona, ItalyTaking people
- Azienda Ospedaliero Universitaria Ospedali RiunitiFoggia, ItalyTaking people
- Azienda Unita Sanitaria Locale Della RomagnaForli', ItalyTaking people
- Centro Cardiologico Monzino S.p.A.Milan, ItalyTaking people
- Ospedale San Raffaele S.r.l.Milan, ItalyTaking people
- Azienda Ospedaliera dei ColliNaples, ItalyTaking people
- Azienda Ospedaliera Universitaria Federico II Di NapoliNaples, ItalyTaking people
- Azienda Ospedaliero Universitaria ParmaParma, ItalyTaking people
- Fondazione IRCCS Policlinico San MatteoPavia, ItalyTaking people
- Azienda Unita Sanitaria Locale Della RomagnaRimini, ItalyTaking people
- Azienda Sanitaria Locale TO3Rivoli, ItalyTaking people
- Fondazione Policlinico Universitario Campus Bio-medico In Forma A Bbreviata FonRome, ItalyTaking people
- Humanitas Mirasole S.p.A.Rozzano, ItalyTaking people
- Azienda Ospedaliero-Universitaria di SassariSassari, ItalyTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record
Print a page for my doctorTrial details
- Who runs it
- Amgen Inc.
- Trial code
- EU 2024-516654-22-00
- Record updated
- 11 November 2026
- Original description
To demonstrate that maridebart cafraglutide is superior to placebo when given as an adjunct to standard of care on the composite endpoint of heart failure (HF) events (hospitalization for HF or urgent HF visits) or death from cardiovascular (CV) disease in participants with HF with preserved ejection fraction (HFpEF) and HF with mildly reduced ejection fraction (HFmrEF) and a body mass index (BMI) ≥ 30 kg/m2Read full original descriptionShow less
A Phase 3 Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Maridebart Cafraglutide on Mortality and Morbidity in Participants Living With Heart Failure With Preserved or Mildly Reduced Ejection Fraction and Obesity (MARITIME-HF)
To demonstrate that maridebart cafraglutide is superior to placebo when given as an adjunct to standard of care on the composite endpoint of heart failure (HF) events (hospitalization for HF or urgent HF visits) or death from cardiovascular (CV) disease in participants with HF with preserved ejection fraction (HFpEF) and HF with mildly reduced ejection fraction (HFmrEF) and a body mass index (BMI) ≥ 30 kg/m2
Inclusion: Age ≥ 18 years (or ≥ legal age within the country if it is older than 18 years) at the time of informed consent; BMI ≥ 30 kg/m2 at randomization; HF diagnosed for at least 30 days with NYHA Class II-IV at the time of informed consent; Managed with HF standard of care therapies consistent with regional clinical practice guidelines, stable for at least 14 days before randomization, according to investigator judgment; Documented LVEF of > 40% measured by any modality within 12 months, before randomization; For participants with a prior diagnosis of T2DM at screening or new diagnosis of T2DM during screening: Treatment of T2DM with diet, exercise, and/or glucose-lowering medications according to local label with stable dosing for at least 14 days prior to randomization.
Exclusion: History of any of the following within 60 days prior to or during screening: Type I (spontaneous) MI, valvular replacement or repair, coronary revascularization, coronary artery bypass graft surgery or other major cardiovascular surgery, stroke; In the opinion of the investigator, use within 90 days prior to or during the screening period of medications that may cause significant weight gain; Any of the following psychiatric history: -History of unstable major depressive disorder or other severe psychiatric disorder within 2 years prior to screening or during the screening period -Lifetime history of suicide attempt -History of non-suicidal self-injury within 5 years prior to screening or during the screening period; Currently receiving treatment in another investigational device or drug study, or less than 90 days (or 5 half-lives, whichever is longer) prior to randomization since ending treatment in another investigational device or drug study(ies); Previous or planned participation in a study that includes maridebart cafraglutide or AMG 598; Hospitalization with a primary diagnosis of decompensated HF which required IV loop diuretic treatment, within 30 days prior to randomization; SBP ≥ 180 mmHg during the screening period, or on three or more blood pressure-lowering drugs with a SBP > 160 mmHg during the screening period; Planned bariatric surgery at the time of screening, or performed within 180 days of Screening; History of acute pancreatitis in the 180 days before screening or during the screening period; Severe, concomitant disease that is expected to reduce life expectancy to < 1 year; Use of any GLP-1 RA, GIP agonists or antagonists, or amylin analogs within 90 days prior to or during the screening period or planned use during the conduct of the study; Treatment with continuous SC insulin therapy during screening or participants on intensive insulin therapy guided by carbohydrate counting; Use within 90 days prior to or during the screening period of medications prescribed for weight loss; Type 1 diabetes mellitus, or any type of diabetes with the exception of T2DM or history of gestational diabetes; Heart failure due to: hypertrophic cardiomyopathy (obstructive and non obstructive), infiltrative cardiomyopathy (including cardiac sarcoid, lymphoma, cardiac amyloid, endomyocardial fibrosis), active or chronic myocarditis, constrictive pericarditis, cardiac tamponade, arrhythmogenic right ventricular or left ventricular cardiomyopathy/dysplasia, uncorrected primary valvular heart disease, clinically significant congenital heart disease; Any personal lifetime history of, or family history (first-degree relative[s]) of medullary thyroid carcinoma or MEN-2; History of malignancy within the last 5 years prior to screening or during the screening period; History of chronic pancreatitis; Family (first-degree relative[s]) or personal history of medullary thyroid carcinoma or MEN-2; Obesity induced by specific endocrinologic disorders or monogenetic or syndromic forms of obesity; Recipient of heart transplant or listed for any other major organ transplant, listed for heart transplant, or anticipated to receive chronic mechanical circulatory support or heart transplantation within 12 months from randomization; History of any other condition that, in the opinion of the investigator, may preclude the participant from following the protocol and completing the study; For participants with a prior diagnosis of T2DM (including those diagnosed during screening): -HbA1c > 10.0% (86 mmol/mol) at screening -Uncontrolled diabetes requiring immediate therapy at randomization in the judgement of the investigator -History of diabetic ketoacidosis or hyperosmolar state/coma within 12 months before randomization -One or more episodes of severe hypoglycemia within 6 months before randomization and/or history of hypoglycemia unawareness -History or presence of either proliferative diabetic retinopathy, or diabetic maculopathy, or severe non-proliferative diabetic retinopathy; or currently receiving or planning to receive treatment for diabetic retinopathy and/or macular edema; Acute or chronic hepatitis; signs and symptoms of any liver disease other than MSALD; or ALT > 3.0 x ULN, during screening or TBL > 1.8 x ULN during screening; eGFR < 20 mL/min/1.73 m2 according to the 2021 CKD-EPI creatinine (Cr)-cystatin C equation or receiving dialysis at screening; Calcitonin ≥ 50 ng/L (pg/mL) at screening; Clinically significant gastric-emptying abnormality; Hospitalized with acute decompensated HF at the time of or during the screening period.