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MARITIME-HF

Trial Overview

Official Title

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 Obesity and Heart Failure

Study Purpose

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

Diagnosis

BMI ≥ 30 kg/m2 Chronic symptomatic HFpEF or HFmrEF, defined as LVEF ≥ 40% at screening or within 180 days before screening

Eligibility

Stable diet and medical treatment

Intervention

Maridebart Cafraglutide / AMG 133

Key Participation Requirements
Trial Location(s)
Gender
Male & Female
Age
19+
Enrollment Status
Available
Phase
Phase III
Methodist Health System Trial Code
NCT07037459
Related Specialties