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Active Surveillance SNEP Assay Registry Trial for Prostate Cancer
NCT04052048 · View on ClinicalTrials.gov ↗
Study Summary
A multi-center, prospective active surveillance registry trial assessing the performance of a non-invasive blood test for indolent prostate cancer disease management.
Conditions Studied
Interventions
- DIAGNOSTIC_TEST Subtraction Normalized Expression of Phagocytes Blood Test
Study Locations (1)
Michigan
- Comprehensive Urology — Royal Oak
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 2,000 participants |
| Start Date | 2019-09-09 |
| Est. Completion | 2029-09-30 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04052048
The ClinicalTrials.gov registry entry for NCT04052048 describes a study currently listed as recruiting. 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 2,000 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Immunis.AI, 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 1 condition, with Prostate Cancer Aggressiveness appearing as the primary indexed condition, and to 1 intervention — of which Subtraction Normalized Expression of Phagocytes Blood Test 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: NCT04052048 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 NCT04052048 about?
NCT04052048 is a clinical study titled "Active Surveillance SNEP Assay Registry Trial for Prostate Cancer". A multi-center, prospective active surveillance registry trial assessing the performance of a non-invasive blood test for indolent prostate cancer disease management.
What is the current status of trial NCT04052048?
This trial is currently recruiting. The enrollment target is 2,000 participants. The study started on 2019-09-09. Estimated completion is 2029-09-30.
What conditions does trial NCT04052048 study?
This clinical trial studies the following conditions: Prostate Cancer Aggressiveness. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04052048?
The interventions under investigation include: Subtraction Normalized Expression of Phagocytes Blood Test (DIAGNOSTIC_TEST). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04052048?
This trial is sponsored by Immunis.AI, 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 NCT04052048 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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