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suPAR Michigan M2C2 Heterogeneity Validation Cohort Study
NCT07466524 · View on ClinicalTrials.gov ↗
Study Summary
This is a retrospective, non interventional cohort study using stored plasma samples from appoximately 300 adults hospitalized with confirmed COVID 19. Baseline suPAR measured using the suPARnostic TurbiLatex assay on the Roche cobas c501.
Conditions Studied
Interventions
- DIAGNOSTIC_TEST suPARnostic® TurbiLatex Assay on Roche cobas c501
Study Locations (1)
Michigan
- Michigan state university, Department of Biostatistics — Ann Arbor
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 367 participants |
| Start Date | 2020-02-01 |
| Est. Completion | 2022-10-19 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07466524
The ClinicalTrials.gov registry entry for NCT07466524 describes a study currently listed as completed. It is categorized as an unspecified phase, 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 367 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is ViroGates A/S, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 3 conditions, with COVID-19 appearing as the primary indexed condition, and to 1 intervention — of which suPARnostic® TurbiLatex Assay on Roche cobas c501 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: NCT07466524 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 NCT07466524 about?
NCT07466524 is a clinical study titled "suPAR Michigan M2C2 Heterogeneity Validation Cohort Study". This is a retrospective, non interventional cohort study using stored plasma samples from appoximately 300 adults hospitalized with confirmed COVID 19. Baseline suPAR measured using the suPARnostic TurbiLatex assay on the Roche cobas c501.
What is the current status of trial NCT07466524?
This trial is currently completed. The enrollment target is 367 participants. The study started on 2020-02-01. Estimated completion is 2022-10-19.
What conditions does trial NCT07466524 study?
This clinical trial studies the following conditions: COVID-19, Acute Respiratory Distress Syndrome, Severe Respiratory Distress Syndrome. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT07466524?
The interventions under investigation include: suPARnostic® TurbiLatex Assay on Roche cobas c501 (DIAGNOSTIC_TEST). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT07466524?
This trial is sponsored by ViroGates A/S, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT07466524 being conducted?
This trial has 1 study location across Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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