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COMPLETED
NCT05562063
PHASE4

Sotagliflozin in Heart Failure With Preserved Ejection Fraction (HFpEF) Patients

Sponsor: Juan Badimon

View on ClinicalTrials.gov

Summary

The clinical benefits of the dual Sodium-Glucose cotransporter (SGLT) 1 and 2-inhibition have recently been reported in two clinical trials. The SOLOIST reported the benefits of sotagliflozin in Type-2 Diabetes Mellitus (T2DM) patients hospitalized for worsening of Heart Failure (HF), while the SCORED involved T2DM patients with Chronic Kidney Disease (CKD). It is worth noting that not only did the event curves separate within the first week post-treatment, but the effects of sotagliflozin on HF-related outcomes were observed regardless of Left Ventricular Ejection Fraction (LVEF) values and did not seem to attenuate with increasing LVEF as seen with empagliflozin and sacubitril/valsartan. Despite the favorable outcomes, the mechanism(s) of action through which sotagliflozin exerts these benefits remains unclear. The present study aims to investigate the potential (non-glucose dependent) "cardio-renal" pleiotropic effects of sotagliflozin in a mechanistic, randomized, double blind, placebo-control trial in HF patients with preserved ejection fraction (HFpEF). Comparisons between treatment groups will be made using cardiac MRI, CPET, 6-MWT and KCCQ-12.

Official title: SOTA-P-CARDIA Trial: A Randomized Trial of Sotagliflozin in HFpEF Patients Without Diabetes

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

88

Start Date

2022-10-26

Completion Date

2025-06-04

Last Updated

2026-06-24

Healthy Volunteers

No

Interventions

DRUG

Sotagliflozin

Daily administration of sotagliflozin (2x200 mg, PO, OD) for 6 months.

DRUG

Placebo

Matching placebo for 6 months.

Locations (1)

Icahn School of Medicine at Mount Sinai

New York, New York, United States