This trial will examine if maridebart cafraglutide as an adjunct to standard of care will lead to a reduction in heart failure (HF) events such as HF hospitalizations and urgent HF visits, cardiovascular (CV) deaths and improvement in HF symptoms in participants with HF with preserved ejection fraction (HFpEF) and HF with mildly reduced ejection fraction (HFmrEF) who are obese. This is a phase 3, global, multicenter, 2-part trial with a double-blind period and an open-label extension (OLE). The trial is event-driven, and Part 1 will conclude when approximately 850 primary endpoint events have occurred.
Maridebart cafraglutide will be administered SC.
Placebo will be administered SC.
CABA, Buenos Aires, Argentina
CABA, Buenos Aires, Argentina
CABA, Buenos Aires, Argentina
CABA, Buenos Aires, Argentina
CABA, Buenos Aires, Argentina
Ciudad Autonoma de Buenos Aires, Buenos Aires, Argentina
Ciudad Autonoma de Buenos Aires, Buenos Aires, Argentina
Ciudad Autonoma de Buenos Aires, Buenos Aires, Argentina
Morón, Buenos Aires, Argentina
Ramos Meija, Buenos Aires, Argentina
San Nicolás de los Arroyos, Buenos Aires, Argentina
San Nicolás de los Arroyos, Buenos Aires, Argentina
Villa María, Córdoba Province, Argentina
Rosario, Santa Fe Province, Argentina
Rosario, Santa Fe Province, Argentina
San Miguel de Tucumán, Tucumán Province, Argentina
San Miguel de Tucumán, Tucumán Province, Argentina
Córdoba, Argentina
Rosario, Argentina
Santa Fe, Argentina
Zárate, Argentina