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临床试验/NCT06618976
NCT06618976已完成4 期

SOTA-THROMBOSIS: Antithrombotic Activities of Sotagliflozin vs. Empagliflozin

Icahn School of Medicine at Mount Sinai1 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2025年2月25日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
17
试验地点
1
主要终点
Thrombus size

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects are eligible if they meet all of the following criteria:
  • Male or female volunteers older than 18 years old.
  • Disease-free as assessed by medical history and physical examination.
  • Ability to provide signed informed consent.

排除标准

  • Subjects will be excluded if they meet any of the following criteria:
  • Pregnant or lactating women
  • History of clinically relevant cardiovascular, pulmonary, hepatic, gastrointestinal, renal, metabolic, hematologic, neurologic, respiratory or psychiatric disease, bleeding, acute infectious disease or signs of acute illness.
  • Use of medication within one month prior to study drug administration or within six times the elimination half-life (whichever is longer), except for oral contraceptives or occasional use of acetaminophen or an antihistamine.
  • History of drug abuse or alcohol consumption >20 g/day [125 ml (30ml=1oz) glass of 10% wine = 12.5 g, 40 mL aperitif of 40% = 17 g, 250 mL glass of 6% beer = 15g]
  • Loss of >400 mL blood or blood donation within 3 months.
  • Conditions associated with hemorrhagic risk, e.g., frequent epistaxis, gastrointestinal ulcer, hemorrhagic vascular lesions, recent surgery.

研究组 & 干预措施

Sotagliflozin then Empagliflozin

Other

Subjects randomized to 'Arm A' will receive 1-month of 'Sotagliflozin' treatment first and then 1-month of 'Empagliflozin' treatment second, separated by a 1-month of washout period.

干预措施: Empagliflozin (Drug)

Sotagliflozin then Empagliflozin

Other

Subjects randomized to 'Arm A' will receive 1-month of 'Sotagliflozin' treatment first and then 1-month of 'Empagliflozin' treatment second, separated by a 1-month of washout period.

干预措施: Sotagliflozin (Drug)

Empagliflozin then Sotagliflozin

Other

Subjects randomized to 'Arm B' will receive1-month of 'Empagliflozin' treatment first and then1-month of 'Sotagliflozin' treatment second, separated by a 1-month of washout peri od

干预措施: Sotagliflozin (Drug)

Empagliflozin then Sotagliflozin

Other

Subjects randomized to 'Arm B' will receive1-month of 'Empagliflozin' treatment first and then1-month of 'Sotagliflozin' treatment second, separated by a 1-month of washout peri od

干预措施: Empagliflozin (Drug)

结局指标

主要结局

Thrombus size

时间窗: Baseline and end of each treatment period (1 month and 3 months)

Changes in blood thrombogenicity (thrombus size) from baseline to post-treatment

次要结局

  • Clot formation size(Baseline and end of each treatment period (1 month and 3 months))
  • Platelet aggregation(Baseline and end of each treatment period (1 month and 3 months))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Juan Badimon

Professor of Medicine

Icahn School of Medicine at Mount Sinai

研究点 (1)

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