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NCT04799392 · ClinicalTrials.gov registry record · NA

NOWDx Test for the Detection of Antibodies to COVID-19 in Lay Persons

A NA study, sponsored by NOWDiagnostics.

Terminated
Registry status
NA
Development phase
50
Enrollment target

NCT04799392: Clinical Trial NA study, sponsored by NOWDiagnostics.

NCT04799392 is a NA study that was terminated before completion, run by NOWDiagnostics. The registered enrollment target is 50 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04799392, a NA study, was terminated before completion, sponsored by NOWDiagnostics.

TERMINATED
Registry status
NA
Development phase
50 participants
Enrollment target

Study Summary

This study is designed to compare the performance of the NOWDx COVID-19 Test to an emergency use authorized PCR test result. The intent is to show the rapid test device is comparable to a currently marketed device. The NOWDx COVID-19 Test is an in vitro lateral flow immunoassay intended for qualitative detection of total antibodies to SARS-CoV-2 in human fingerstick whole blood at the Point of Care (POC); i.e. in patient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation; and at home.

Primary Outcome

Calculate positive percent agreement (PPA) and negative percent agreement (NPA) between NOWDx COVID-19 Test and emergency use authorized or FDA cleared COVID-19 PCR test.

Interventions

  • DEVICE NOWDx COVID-19 Test

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2021-04-01
Est. Completion 2021-10-28
Phase NA
NOWDiagnostics

4 total trials

Why NCT04799392 stopped before completion

NCT04799392 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 1 intervention - of which NOWDx COVID-19 Test is the first listed.

NCT04799392 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04799392 about?

NCT04799392 is a clinical study titled "NOWDx Test for the Detection of Antibodies to COVID-19 in Lay Persons". This study is designed to compare the performance of the NOWDx COVID-19 Test to an emergency use authorized PCR test result. The intent is to show the rapid test device is comparable to a currently marketed device. The NOWDx COVID-19 Test is an in vitro lateral flow immunoassay intended for qualitat...

What is the current status of trial NCT04799392?

This trial is currently terminated. It is a NA study. The enrollment target is 50 participants. The study started on 2021-04-01. Estimated completion is 2021-10-28.

What interventions are being tested in trial NCT04799392?

The interventions under investigation include: NOWDx COVID-19 Test (DEVICE).

Who is sponsoring clinical trial NCT04799392?

This trial is sponsored by NOWDiagnostics, which has 4 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04799392's enrollment target sits among peer trials

50 1279th of 2000 higher than 622 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT04799392, the US trial registry maintained by the National Library of Medicine. NCT04799392 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.