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QIAGEN Launches Portable Digital SARS-CoV-2 Antigen Test That Can Accurately Analyze Over 30 Samples Per Hour

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QIAGEN has launched the QIAreach™ SARS-CoV-2 Antigen Test in the U.S., enabling rapid detection of SARS-CoV-2 antigens in 2-15 minutes for active infections. Developed with Ellume, the test can process over 30 samples per hour and offers digital results without subjective interpretation. An EUA application for symptomatic patients has been submitted, with plans for a POC claim later this year. The test addresses the need for scalable and accurate antigen testing as part of COVID-19 strategies, complementing PCR testing for higher throughput.

Positive
  • Launch of a new portable digital test for SARS-CoV-2 antigen detection.
  • Ability to process over 30 swab samples per hour.
  • Offers digital results, eliminating subjective interpretation.
  • Addresses the increasing demand for scalable testing solutions.
Negative
  • None.

HILDEN, Germany & GERMANTOWN, Md.--()--QIAGEN (NYSE: QGEN; Frankfurt Prime Standard: QIA) has started commercialization of a portable digital test in the United States that can be used by laboratories to detect SARS-CoV-2 antigens in people with active infections in 2-15 minutes. A point of care (POC) claim will be added and EUA amended later this year.

The QIAreach™ SARS-CoV-2 Antigen Test, developed in partnership with the Australian digital diagnostics company Ellume, sets new standards in scalability, validation and flexibility by processing more than 30 swab samples per hour, providing digital test results that do not require subjective interpretation, and allowing antibody tests to run simultaneously with antigen tests. This flexibility will be particularly valuable when vaccines are introduced.

QIAGEN has begun marketing and distributing QIAreach™ SARS-CoV-2 Antigen Test in the United States after applying for FDA emergency use authorization (EUA) for symptomatic patients. CE-IVD registration for European Union and other markets is expected as early as by the end of the year.

“As existing approaches often lack scalability and accuracy, antigen testing is playing an increasingly important role in national testing strategies as a complementary tool to PCR, the gold-standard for detecting active COVID-19 infections,” said Thierry Bernard, Chief Executive Officer of QIAGEN. “QIAreach SARS-CoV Antigen is a fast, digital and easy to use test that makes use of sensitive nanoparticle technology from Ellume. In as little as two minutes it allows objective reading of test results that provide clear qualitative interpretation. And it addresses the growing need for higher throughput testing for SARS-CoV-2 antigen by processing up to eight tests per hub simultaneously.”

Please find the full press release here

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Contacts

QIAGEN

Investor Relations
e-mail: ir@QIAGEN.com

John Gilardi
+49 2103 29 11711

Phoebe Loh
+49 2103 29 11457

Public Relations

e-mail: pr@QIAGEN.com

Thomas Theuringer
+49 2103 29 11826

Robert Reitze
+49 2103 29 11676

FAQ

What is the QIAreach™ SARS-CoV-2 Antigen Test?

The QIAreach™ SARS-CoV-2 Antigen Test is a portable digital test that detects SARS-CoV-2 antigens in 2-15 minutes, allowing for rapid identification of active infections.

Who developed the QIAreach™ SARS-CoV-2 Antigen Test?

The test was developed by QIAGEN in partnership with the Australian digital diagnostics company Ellume.

How many samples can the QIAreach™ test process per hour?

The QIAreach™ SARS-CoV-2 Antigen Test can process more than 30 samples per hour.

What is the EUA status of the QIAreach™ test?

QIAGEN has submitted an application for FDA emergency use authorization (EUA) for the QIAreach™ test for symptomatic patients.

When is the point of care claim expected for the QIAreach™ test?

The point of care (POC) claim for the QIAreach™ SARS-CoV-2 Antigen Test is expected to be added later this year.

QIAGEN N.V.

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