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 screeningEligibility
Stable diet and medical treatment
Intervention
Maridebart Cafraglutide / AMG 133
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Key Participation Requirements
Trial Location(s)
Gender
Male & Female
Age
19+
Enrollment Status
Available
Phase
Phase III
Methodist Health System Trial Code
NCT07037459