Primary Objective: To compare the effect of sotagliflozin to placebo on the total occurrences of cardiovascular (CV) death, hospitalization for heart failure (HHF), and urgent visit for heart failure (HF) in hemodynamically stable participants after admission for worsening heart failure (WHF) Secondary Objectives: To compare the effects of sotagliflozin to placebo on: * The total occurrences of HHF and urgent visit for HF * The occurrence of CV death * The occurrence of all-cause mortality * The total occurrences of CV death, HHF, urgent visit for HF, non-fatal myocardial infarction (MI), and non-fatal stroke * Change in Kansas City Cardiomyopathy Questionnaire-12(KCCQ-12) score * Change in estimated glomerular filtration rate (eGFR)
The estimated study duration for a given participants will be approximately 3 to 24 months.
Pharmaceutical form: tablet Route of administration: oral
Pharmaceutical form: tablet Route of administration: oral
Caba, Argentina
Caba, Argentina
Capital Federal, Argentina
Ciudad de Buenos Aires, Argentina
Corrientes, Argentina
Corrientes, Argentina
Córdoba, Argentina
Córdoba, Argentina
Córdoba, Argentina
Córdoba, Argentina
Córdoba, Argentina
La Plata, Argentina
La Plata, Argentina
Merlo, Argentina
Morón, Argentina
Olivos, Argentina
Quilmes, Argentina
Rosario, Argentina
Rosario, Argentina
Salta, Argentina
San Martín, Argentina
San Miguel de Tucumán, Argentina
San Miguel de Tucumán, Argentina
San Miguel de Tucumán, Argentina
Santa Fe, Argentina
Santa Fe, Argentina
Villa Belgrano, Argentina
Villa María, Argentina