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
| Type | Name | Description |
|---|---|---|
| DRUG | Sotagliflozin (SOTA) followed by 3 drugs in a random order | 400 mg/day SOTA Each drug will be given daily for 2 weeks. |
| DRUG | Aspirin followed by 3 drugs in a random order | 81 mg/day Aspirin Each drug will be given daily for 2 weeks. |
| DRUG | Clopidogrel followed by 3 drugs in a random order | 75 mg/day clopidogrel Each drug will be given daily for 2 weeks. |
| DRUG | Eliquis followed by 3 drugs in a random order | 5 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
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT06933056. Inclusion in this directory is not an endorsement.