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RECRUITING Early Phase 1

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

NCT06933056 · View on ClinicalTrials.gov ↗

Study 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.

Interventions

  • DRUG Sotagliflozin (SOTA) followed by 3 drugs in a random order
  • DRUG Aspirin followed by 3 drugs in a random order
  • DRUG Clopidogrel followed by 3 drugs in a random order
  • DRUG Eliquis followed by 3 drugs in a random order

Study Locations (1)

Michigan

  • University of Michigan — Ann Arbor

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2025-09-02
Est. Completion 2026-09
Phase Early Phase 1

Sponsor

University of Michigan

1,126 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06933056

The ClinicalTrials.gov registry entry for NCT06933056 describes a study currently listed as recruiting. It is categorized as Early Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Michigan, which has 1,126 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Platelet Function and Reactivity Tests appearing as the primary indexed condition, and to 4 interventions — of which Sotagliflozin (SOTA) followed by 3 drugs in a random order is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06933056 reports 1 study location spanning 1 distinct geographic area — top geographies include Michigan. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06933056 about?

NCT06933056 is a clinical study titled "Comparison of Antiplatelet Effects of Sotagliflozin to FDA-approved Antiplatelet Drugs". This study will identify the potential benefits of regulating platelet activation with sotagliflozin compared to other FDA-approved drugs known to limit platelet activation.

What is the current status of trial NCT06933056?

This trial is currently recruiting. It is a Early Phase 1 study. The enrollment target is 20 participants. The study started on 2025-09-02. Estimated completion is 2026-09.

What conditions does trial NCT06933056 study?

This clinical trial studies the following conditions: Platelet Function and Reactivity Tests. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06933056?

The interventions under investigation include: Sotagliflozin (SOTA) followed by 3 drugs in a random order (DRUG), Aspirin followed by 3 drugs in a random order (DRUG), Clopidogrel followed by 3 drugs in a random order (DRUG), Eliquis followed by 3 drugs in a random order (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06933056?

This trial is sponsored by University of Michigan, which has 1,126 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06933056 being conducted?

This trial has 1 study location across Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial