bioMérieux Serology Tests for SARS-CoV-2 on VIDAS® Undergo Validation Preceding Imminent Launch
06 Mai 2020 - 7:00AM
Business Wire
Regulatory News:
bioMérieux (Paris:BIM), a world leader in the field of in vitro
diagnostics, today announced performance validation and the
upcoming launch of VIDAS® anti-SARS-CoV-2 serology tests to detect
antibodies in people who have been exposed to the SARS-CoV-2 that
causes the COVID-19 disease.
Building on years of experience in developing immunoassays,
bioMérieux worked closely with several hospitals to develop and
validate the performances of two tests. VIDAS® anti-SARS-CoV-2 IgM
and anti-SARS-CoV-2 IgG will identify in less than 30 minutes the
presence of antibodies in people who have been infected with
SARS-CoV-2. In this context, clinical specificity is particularly
important to ensure that testing of uninfected individuals
consistently shows a negative result. Both VIDAS® anti-SARS-CoV-2
IgM and anti-SARS-CoV-2 IgG demonstrated excellent clinical
specificity data.
François Lacoste, Executive VP R&D at bioMérieux stated:
“Thanks to the engagement and the experience of our research and
development teams, bioMérieux is now going to launch two new
serology assays to assess the immune response following SARS-CoV-2
infection. These tests will complement our three already launched
molecular tests for the direct detection of the virus. Offering
complementary testing solutions to laboratories is crucial to help
overcome this pandemic. True to its commitment to serve public
health, bioMérieux is one of the few players to propose a complete
diagnostic solution for COVID-19 disease”.
Hospitals and private laboratories can run the tests on
bioMérieux’s VIDAS® analyzers (MINI VIDAS®, VIDAS® and VIDAS® 3)
which are widely available with more than 30 000 systems installed
around the world.
bioMérieux aims to have the VIDAS® anti-SARS-CoV-2 serology
tests available by mid-May as RUO (Research Use Only). They will be
CE marked rapidly thereafter and bioMérieux will file a request for
Emergency Use Authorization (EUA) to the US Food and Drug
Administration.
Thanks to the expertise and a close collaboration between
R&D, industrialization and manufacturing on the same site in
France, bioMérieux is planning on an accelerated ramp-up to produce
several million serology tests per month in the coming weeks.
ABOUT BIOMÉRIEUX GLOBAL RESPONSE TO
COVID-19
bioMérieux already provides several solutions for the molecular
detection of SARS-CoV-2:
- ARGENE® SARS-CoV-2 R-GENE® test (CE-marked on April
10th, under EUA assessment by the FDA): this test relies on the
real-time PCR technology and can be used with most commercially
available amplification PCR-platforms. The SARS-CoV-2 R-GENE® test
allows many patients to be tested simultaneously and provide
results in 4 to 5 hours. It has been developed and is produced in
France.
- BIOFIRE® COVID-19 test (EUA granted on March 23rd,
2020): this test is a fully automated test that provides results
from a patient sample in 45 minutes. It is suitable for use in
emergency situations for critically ill patients. The BIOFIRE®
COVID-19 test was developed with funding from the U.S. Department
of Defense (DoD) and is produced in Utah (USA).
- BIOFIRE® Respiratory Panel 2.1 (RP2.1) (EUA granted on
May 1st, 2020): this new panel includes SARS-CoV-2 in addition to
21 other common respiratory pathogens and delivers results in
approximately 45 minutes. A BIOFIRE® Respiratory Panel 2.1
plus will also be available in international markets and will
include the detection of MERS-Coronavirus in addition to the
SARS-CoV-2 virus. Both panels can be run on the FILMARRAY® 2.0 and
FILMARRAY® TORCH platforms. Tests were developed and are produced
in Utah (USA).
- EMAG® and easyMAG® equipments and associated
reagents are pivotal for the extraction of nucleic acids prior to
the amplification and detection of specific gene sequences. These
systems are in high demand as a means of preparing nucleic acids
from clinical specimens for many SARS-CoV-2 RT-PCR tests available
on the market. Reagents are produced in France, instruments in
Italy.
ABOUT BIOMÉRIEUX
Pioneering Diagnostics
A world leader in the field of in vitro diagnostics for over 55
years, bioMérieux is present in 44 countries and serves more than
160 countries with the support of a large network of distributors.
In 2019, revenues reached €2.7 billion, with over 90% of
international sales.
bioMérieux provides diagnostic solutions (systems, reagents,
software and services) which determine the source of disease and
contamination to improve patient health and ensure consumer safety.
Its products are mainly used for diagnosing infectious diseases.
They are also used for detecting microorganisms in agri-food,
pharmaceutical and cosmetic products.
bioMérieux is listed on the Euronext Paris stock market. Symbol:
BIM – ISIN Code: FR0013280286 Reuters: BIOX.PA/Bloomberg:
BIM.FP
Corporate website: www.biomerieux.com.
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version on businesswire.com: https://www.businesswire.com/news/home/20200505006141/en/
Investor Relations bioMérieux Sylvain Morgeau
Tel.: + 33 4 78 87 51 36 investor.relations@biomerieux.com
Media Relations bioMérieux Aurore Sergeant Tel.: +
33 4 78 87 21 99 media@biomerieux.com
Image Sept Laurence Heilbronn Tel.: + 33 1 53 70 74 64
lheilbronn@image7.fr
Claire Doligez Tel.: + 33 1 53 70 74 48 cdoligez@image7.fr
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