Roche’s response to the COVID-19 pandemic

Coronavirus close up

COVID-19 pandemic

 

Timely availability and fast access to reliable, high quality tests are essential for healthcare systems.

Thomas Schinecker
Chief Executive Officer of Roche Diagnostics

Our commitment to help put a stop to the COVID-19 pandemic

 

Roche is deeply committed to supporting the global response to put an end to the COVID-19 pandemic. Around the world, we are working with urgency, passion and purpose each and every day to deliver high quality tests that are essential for healthcare systems and patients alike.

Detecting SARS-CoV-2 in currently infected patients with high sensitivity

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Laboratory tests

High-throughput PCR testing on cobas® 6800/8800 Systems

 

 

cobas® SARS-CoV-2 Test

Real-time RT-PCR test intended for the qualitative detection of SARS-CoV-2 in nasal, nasopharyngeal and oropharyngeal swab samples from asymptomatic and symptomatic individuals.

 

cobas® SARS-CoV-2 & Influenza A/B Test

Simultaneous qualitative detection and differentiation of SARS-CoV-2, influenza A virus, and/or influenza B virus in nasal or nasopharyngeal swab samples collected from individuals suspected of a respiratory viral infection consistent with COVID-19 by their healthcare provider. 

High-throughput testing on cobas® immunochemistry analyzers

 

Elecsys® SARS-CoV-2 Antigen

The Elecsys® SARS-CoV-2 Antigen is an immunoassay for the qualitative detection of the SARS-CoV-2 nucleocapsid antigens.

Syndromic testing on the ePlex® System

The Respiratory Pathogen Panel 2 (RP2) identifies the most common viral and bacterial organisms associated with upper respiratory infection, including SARS-CoV-2, the virus that causes COVID-19.
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Point of Care tests

Point-of-care PCR testing in just 20 minutes on cobas® Liat® System

 

cobas® SARS-CoV-2 Assay

Authorized for use in screening and testing asymptomatic and symptomatic individuals, cobas® SARS-CoV-2 is a real-time RT-PCR assay intended for the rapid in vitro qualitative detection of SARS-CoV-2.

 

cobas® SARS-CoV-2 & Influenza A/B Assay

For patients presenting with symptoms of respiratory illness or is suspected of a respiratory infection consistent with COVID-19, the cobas® SARS-CoV-2 & Influenza A/B Assay for use with the cobas® Liat® System brings the simultaneous rapid in vitro qualitative detection and differentiation of SARS-CoV-2, influenza A, and influenza B in an automated multiplex real-time RT-PCR assay for use at the point of care.

 

Rapid Antigen Tests

 

SARS-CoV-2 Rapid Antigen Test

The SARS-CoV-2 Rapid Antigen Test is a reliable, rapid chromatographic immunoassay for the qualitative detection of specific antigens of SARS-CoV-2 present in the human nasopharynx.

 

SARS-CoV-2 Rapid Antigen Test Nasal

The SARS-CoV-2 Rapid Antigen Test Nasal is a reliable, rapid chromatographic immunoassay for the qualitative detection of nucleocapsid antigen present in human nasal samples.

 

SARS-CoV-2 Antigen Self Test Nasal

The SARS-CoV-2 Antigen Self Test Nasal provides reliable results for individuals suspected of having COVID-19. The Self Test can be performed by the general public, providing another option for decentralized testing.

Detecting a patient’s immune response to SARS-CoV-2 with high specificity

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Laboratory tests

Antibody tests

 

Elecsys® Anti-SARS-CoV-2 is an immunoassay for the in vitro qualitative detection of antibodies (including IgG) to SARS-CoV-2 in human serum and plasma. The test is intended as an aid in the determination of the immune reaction to SARS-CoV-2.

Elecsys® Anti-SARS-CoV-2 S is an immunoassay for the in vitro quantitative determination of antibodies (including IgG) to the SARS-CoV-2 spike (S) protein receptor binding domain (RBD) in human serum and plasma.

The electrochemiluminescence immunoassay “ECLIA” is intended for use on cobas e immunoassay analyzers.

Elecsys® Anti-SARS-CoV-2

Elecsys® Anti-SARS-CoV-2 S

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Point of Care tests

Rapid Antibody tests

 

The SARS-CoV-2 Rapid Antibody Test is a reliable, rapid chromatographic immunoassay intended for qualitative detection of antibodies (IgM and IgG) to SARS-CoV-2 in human serum, plasma or whole blood.

The test is intended for the use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating prior infection.

SARS-CoV-2 Rapid Antibody Test

Rapid detection or rule-out of co-infections and secondary infections helps improve antibiotic stewardship

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Syndromic testing on the ePlex® System


ePlex® BCID Panels

ePlex® RP2 panel

Because the clinical presentation of COVID-19 and sepsis can be similar, antimicrobial use has increased during the pandemic,1 further driving antimicrobial resistance. Rapid detection or rule-out of bacterial or fungal co-infections and secondary infections can help reduce unnecessary or inadequate antimicrobial therapy.

COVID-19 is accelerating the threat of antimicrobial resistance.3

 

  • Sepsis and COVID-19 can present with similar symptoms, resulting in patients often being treated with broad spectrum antibiotics unnecessarily3
  • Overuse of antibiotics is the primary driver of antibiotic resistance today - most apparent in the treatment of COVID-191
 

When to use which
SARS‑CoV‑2 diagnostic test2

 

Reliable diagnostic tests targeting patients that are currently infected by the virus, as well as those that have an immune response against the virus, are valuable. However, it is important to understand which tests are most suitable to use depending on their intended purpose.

*Whether immunity is gained by individuals who have been infected with SARS-CoV-2 is yet to be confirmed due to the novelty of the virus. Data presented here are based on current scientific understanding of the disease (April 2020)

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Is my sickness COVID‑19?
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How is my body's immune system reacting to the virus?
An overview of SARS-CoV-2 diagnostic tests available
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Abbreviations

 

COVID-19: coronavirus disease 2019

RT-PCR: reverse transcription polymerase chain reaction

 
References
 
  1. Makary, M. et. al. (2021) MedPage Today, https://www.medpagetoday.com/blogs/marty-makary/90795
  2. European Commision (2020). Guidelines on COVID-19 in vitro diagnostic tests and their performance (published 15 April 2020). Available from https://ec.europa.eu/info/sites/info/files/testing_kits_communication.pdf [Accessed April 2020]
  3. Hsu, J. (2020) BMJ;369:m1983, https://www.bmj.com/content/369/bmj.m1983