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Rationale and Design of the SOTA-P-CARDIA Trial (ATRU-V): Sotagliflozin in HFpEF Patients Without Diabetes
Maeve Soto Pérez1,2, Jorge Rodríguez-Capitán3,4, Juan Antonio Requena-Ibáñez5,6
1Atherothrombosis Research Unit, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Pl, New York, NY, 10029-0310, USA. maevesotoperez@gmail.com.
Insights
Sodium-glucose co-transporter 2 inhibitors show promise for heart failure with preserved ejection fraction (HFpEF). The SOTA-P-CARDIA trial investigates sotagliflozin
Area of Science:
- Cardiology
- Pharmacology
- Medical Research
Background:
- Heart failure with preserved ejection fraction (HFpEF) is the most common form of heart failure, associated with high morbidity and mortality.
- Sodium-glucose co-transporter 2 inhibitors (SGLT2i) have emerged as a promising therapy for HFpEF, reducing hospitalizations and cardiovascular mortality.
- Dual SGLT 1/2 inhibitors like sotagliflozin have demonstrated benefits in diabetic HF patients and in preventing HF in those with diabetes and chronic kidney disease.
Purpose of the Study:
- To evaluate the cardiorenal benefits of sotagliflozin in non-diabetic patients with HFpEF.
- To determine if sotagliflozin can be extended to a broader HFpEF population beyond those with diabetes.
- To investigate the efficacy of sotagliflozin in improving cardiac structure and function in non-diabetic HFpEF patients.
Main Methods:
- The SOTA-P-CARDIA trial is a prospective, randomized, double-blinded, placebo-controlled study.
- Non-diabetic patients meeting the universal definition of HFpEF (ejection fraction >50%) will be randomized to receive sotagliflozin or placebo for 6 months.
- The primary outcome is the change in left ventricular mass assessed by cardiac magnetic resonance imaging.
Main Results:
- Primary outcome: Change in left ventricular mass by cardiac magnetic resonance.
- Secondary outcomes include changes in peak VO2, myocardial mechanics, fibrosis, epicardial adipose tissue, 6-minute walk test distance, and quality of life.
- The trial aims to provide insights into the potential benefits of sotagliflozin in non-diabetic HFpEF patients.
Conclusions:
- The SOTA-P-CARDIA trial will assess sotagliflozin's efficacy in non-diabetic HFpEF.
- Results are expected to clarify the role of sotagliflozin in managing HFpEF across different patient populations.
- This research addresses the urgent need for effective therapies in HFpEF.
Abstract:
Heart failure with preserved ejection fraction (HFpEF) is now the most common form of heart failure (HF). This syndrome is associated with an elevated morbi-mortality, and effective therapies are urgently needed. Sodium-glucose co-transporter 2 inhibitors (SGLT2i) are the first pharmacological class that has demonstrated to reduce hospitalization and cardiovascular mortality in large clinical trials in HFpEF. Furthermore, the dual SGLT 1/2 inhibitor sotagliflozin has shown a reduction in cardiovascular outcomes in diabetic HF patients, regardless of ejection fraction Sotagliflozin on Cardiovascular Events in Patients with Type 2 Diabetes Post Worsening Heart Failure (SOLOIST-WHF) Trial, and prevents the development of HF in patients with diabetes and chronic kidney disease Sotagliflozin on Cardiovascular and Renal Events in Patients with Type 2 Diabetes and Moderate Renal Impairment Who Are at Cardiovascular Risk (SCORED) trial. The major objective of the Sotagliflozin in Heart Failure With Preserved Ejection Fraction Patients (SOTA-P-CARDIA) trial (NCT05562063) is to investigate whether the observed cardiorenal benefits of sotagliflozin in HF patients with diabetes can be extended to a non-diabetic population. The SOTA-P-CARDIA is a prospective, randomized, double-blinded, placebo-controlled study that will randomize non-diabetic patients with the universal definition of HFpEF (ejection fraction > 50% assessed the day of randomization). Qualifying patients will be randomized, in blocks of 4, to receive either sotagliflozin or placebo for a period of 6 months. The primary outcome is changes in left ventricular mass by cardiac magnetic resonance from randomization to end of the study between the groups. Secondary end points include changes in peak VO2; myocardial mechanics, interstitial myocardial fibrosis, and volume of epicardial adipose tissue; distance in the 6-min walk test; and quality of life. Finally, the authors expect that this trial will help to clarify the potential benefits of the use of sotagliflozin in non-diabetic HFpEF patients.
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