Icahn School of Medicine at Mount Sinai
New York, 10029, United States
NCT Number: NCT06618976
The availability of Sodium-glucose cotransporter-2 inhibitors (SGLT2-i) has dramatically altered the management of heart failure (HF) patients, independently of their ejection fraction and glycemic status. A meta-analysis of 57 studies comparing SGLT2-I monotherapy vs. placebo or active comparator showed reductions in major cardiovascular events, but no impact on atherothrombotic events. In fact, a non-significant increase in the risk for non-fatal stroke was observed. Similar trend observed in multiple trials indicate a SGLT2-i class effect. Sotagliflozin is the first dual SGLT1/2 receptor inhibitor, that was shown to significantly reduce atherothrombotic events compared with placebo in diabetic HF patients, suggesting that dual SGLT1/2 inhibitor may have additional properties vs. SGLT2-i. The hypothesis of this study is that dual SGLT1/2 inhibition by sotagliflozin improves thrombogenic profile (i.e. reduces thrombus formation), which could make it a safer and more effective treatment option for cardiovascular (CV) patients than SGLT2-i. To test the hypothesis, the researchers will compare the antithrombotic activity of sotagliflozin vs. empagliflozin in healthy volunteers using a randomized, cross-over study design, where each participant will receive both study treatments (sotagliflozin and empagliflozin) separated by a washout period. Treatment effects will be assessed by measuring ex vivo thrombus formation using the Badimon Perfusion chamber, platelet aggregation using Multiplate Analyzer, and Thromboelastometry using RoTEM Gamma. Study assessments will be performed before initiating (baseline/pre-treatment) and after completion of each treatment.
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Notify Me18 year and older
All sexes
Interventional
Phase 4
New York, 10029, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Subjects are eligible if they meet all of the following criteria:
Exclusion criteria
Subjects will be excluded if they meet any of the following criteria:
Sotagliflozin 400 mg, P.O. once daily for 1 month.
Empagliflozin 10 mg, P.O. once daily for 1 month.
Time frame: Baseline and end of each treatment period (1 month and 3 months)
Changes in blood thrombogenicity (thrombus size) from baseline to post-treatment
Time frame: Baseline and end of each treatment period (1 month and 3 months)
A platelet aggregation is a blood test that looks at the reactivity of platelets.
Time frame: Baseline and end of each treatment period (1 month and 3 months)
The size of the clot will be assessed in whole blood samples using a thromboelastometry
Icahn School of Medicine at Mount Sinai
Other
SOTA-THROMBOSIS: Antithrombotic Activities of Sotagliflozin vs. Empagliflozin
Acronym: SOTATHROMBUS
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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