Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06933056

Comparison of Antiplatelet Effects of Sotagliflozin to FDA-approved Antiplatelet Drugs

Comparison of Antiplatelet Effects of Sotagliflozin to FDA-approved Antiplatelet Drugs: an Interventional Study

Status
Recruiting
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
University of Michigan · Academic / Other
Sex
All
Age
18 Years – 79 Years
Healthy volunteers
Accepted

Summary

This study will identify the potential benefits of regulating platelet activation with sotagliflozin compared to other FDA-approved drugs known to limit platelet activation.

Conditions

Interventions

TypeNameDescription
DRUGSotagliflozin (SOTA) followed by 3 drugs in a random order400 mg/day SOTA Each drug will be given daily for 2 weeks.
DRUGAspirin followed by 3 drugs in a random order81 mg/day Aspirin Each drug will be given daily for 2 weeks.
DRUGClopidogrel followed by 3 drugs in a random order75 mg/day clopidogrel Each drug will be given daily for 2 weeks.
DRUGEliquis followed by 3 drugs in a random order5 mg orally twice daily Eliquis Each drug will be given daily for 2 weeks.

Timeline

Start date
2025-09-02
Primary completion
2026-09-01
Completion
2026-09-01
First posted
2025-04-18
Last updated
2025-09-15

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT06933056. Inclusion in this directory is not an endorsement.