QIAGEN and Helix Launch Exclusive Partnership to Advance Next-Generation Sequencing Companion Diagnostics in Hereditary Diseases
05 Januar 2023 - 10:05PM
Business Wire
- Partnership to leverage the Helix® Laboratory Platform
powered by QIAGEN’s biopharma relationships, NGS capabilities, and
global regulatory expertise
- Addressing health burden in neuro-degenerative diseases,
cardio-vascular diseases, and auto-immune and inflammatory diseases
that affect hundreds of millions globally
- Combined offerings include accelerated patient recruitment,
real world evidence and diagnostic solutions using NGS and PCR
technologies
QIAGEN (NYSE:QGEN; Frankfurt Prime Standard: QIA) today
announced an exclusive strategic partnership with California-based
population genomics leader Helix to advance companion diagnostics
for hereditary diseases.
As the development of precision medicines accelerates, so does
the need for companion diagnostics devices and tests detecting
clinically relevant genetic abnormalities. These diagnostics help
guide clinical decision-making by identifying patients most likely
to benefit – or be at increased risk – from a particular
therapeutic product. Principally used in oncology to date,
companion diagnostics that employ whole exome sequencing are widely
believed to have great potential in hereditary disease areas such
as cardiovascular, metabolic, neuro-degenerative, and auto-immune
diseases.
Under the agreement announced today, QIAGEN will be the
exclusive marketing and contracting partner in the U.S. for Helix’s
companion diagnostic services. The partnership will leverage the
Helix® Laboratory Platform, which was granted the first-ever U.S.
Food & Drug Administration de novo class II authorization for a
whole exome sequencing platform. This brings a new innovative
solution to biopharmaceutical customers in support of hereditary
disease therapies, complementing solutions both companies already
provide such as Helix’s population genomics programs and QIAGEN’s
diagnostic expertise, QIAseq Human Exome Kits and global reach
supporting research initiatives outside the U.S.
A pioneer in precision medicine, QIAGEN has more than 30 master
collaboration agreements with global pharmaceutical and
biotechnology companies to develop and commercialize companion
diagnostic tests for their drug candidates. QIAGEN’s companion
diagnostic offerings encompass technologies from next-generation
sequencing (NGS) to polymerase chain reaction (PCR) and digital PCR
(dPCR), sample types from liquid biopsy to tissue, and disease
areas from cancer to Parkinson’s – including 11 FDA-approved PCR
based companion diagnostics and a collaboration with Neuron23
announced in September 2022 to develop an NGS-based companion
diagnostic for a novel Parkinson’s disease drug.
“This partnership represents another step toward bringing the
power of companion diagnostics to hereditary diseases by powering
Helix’s leading products with QIAGEN’s extensive pharma and
biopharma relationships, NGS capabilities, and global regulatory
expertise,” said Thierry Bernard, Chief Executive Officer of
QIAGEN. “Access to a genomic database can help researchers find
patients with particular biomarker signatures almost
instantaneously, making trial recruitment a matter of months
instead of years.”
“Helix’s technology and regulatory capabilities coupled with
QIAGEN’s well-established worldwide companion diagnostic
development capabilities results in a powerful partnership that
will allow us to expand critical access to genomic testing for both
patients and providers working daily to fight life-threatening
conditions,” said Helix CEO and Co-Founder, James Lu, MD, PhD.
“QIAGEN’s mission to fill the clinical gap for patient access and
provide technology platform options to address the needs of
physicians to target treatment with genomic medicine is well in
line with our mission.”
Helix has built an end-to-end platform that enables health
systems, life sciences companies, and payers to advance genomic
research and accelerate the integration of genomic data into
clinical care. Helix has partnered with leading health systems to
enable population genomics programs of at least 100,000 patients
each across the U.S. These programs dramatically accelerate patient
identification and recruitment for clinical trials in hereditary
diseases such as Parkinson’s, cardiovascular or inflammatory
disease like non-alcoholic steatohepatitis (NASH), power real-world
data (RWD) or real-world evidence (RWE) services and insights, and
bring deep genetic expertise and methodologies to examine
sub-cohorts within both drug discovery and a clinical trial.
About Helix
Helix is the leading population genomics and viral surveillance
company operating at the intersection of clinical care, research,
and data analytics. Helix enables health systems, life sciences
companies, payers, and government partners to accelerate the
integration of genomic data into patient care and public health
decision making. Through its human and viral genomic programs,
Helix supports the therapeutic development lifecycle by
accelerating clinical trials and by providing real-world data and
real-world evidence services that generate high value insights
related to hereditary and infectious disease therapies. Learn more
at www.helix.com.
About QIAGEN
QIAGEN N.V., a Netherlands-based holding company, is the leading
global provider of Sample to Insight solutions that enable
customers to gain valuable molecular insights from samples
containing the building blocks of life. Our sample technologies
isolate and process DNA, RNA and proteins from blood, tissue and
other materials. Assay technologies make these biomolecules visible
and ready for analysis. Bioinformatics software and knowledge bases
interpret data to report relevant, actionable insights. Automation
solutions tie these together in seamless and cost-effective
workflows. QIAGEN provides solutions to more than 500,000 customers
around the world in Molecular Diagnostics (human healthcare),
Applied Testing (primarily forensics), Pharma (pharma and biotech
companies) and Academia (life sciences research). As of September
30, 2022, QIAGEN employed more than 6,200 people in over 35
locations worldwide. Further information can be found at
http://www.qiagen.com.
Forward-Looking Statement
Certain statements contained in this press release may be
considered forward-looking statements within the meaning of Section
27A of the U.S. Securities Act of 1933, as amended, and Section 21E
of the U.S. Securities Exchange Act of 1934, as amended. To the
extent that any of the statements contained herein relating to
QIAGEN's products, collaborations markets, strategy or operating
results, including without limitation its expected adjusted net
sales and adjusted diluted earnings results, are forward-looking,
such statements are based on current expectations and assumptions
that involve a number of uncertainties and risks. Such
uncertainties and risks include, but are not limited to, risks
associated with management of growth and international operations
(including the effects of currency fluctuations, regulatory
processes and dependence on logistics), variability of operating
results and allocations between customer classes, the commercial
development of markets for our products to customers in academia,
pharma, applied testing and molecular diagnostics; changing
relationships with customers, suppliers and strategic partners;
competition; rapid or unexpected changes in technologies;
fluctuations in demand for QIAGEN's products (including
fluctuations due to general economic conditions, the level and
timing of customers' funding, budgets and other factors); our
ability to obtain regulatory approval of our products; difficulties
in successfully adapting QIAGEN's products to integrated solutions
and producing such products; the ability of QIAGEN to identify and
develop new products and to differentiate and protect our products
from competitors' products; market acceptance of QIAGEN's new
products and the integration of acquired technologies and
businesses. For further information, please refer to the
discussions in reports that QIAGEN has filed with, or furnished to,
the U.S. Securities and Exchange Commission (SEC).
Source: QIAGEN N.V. Category: Corporate
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version on businesswire.com: https://www.businesswire.com/news/home/20230105005492/en/
Investor Relations John Gilardi, +49 2103 29 11711 Phoebe
Loh, +49 2103 29 11457 e-mail: ir@QIAGEN.com Public
Relations Thomas Theuringer, +49 2103 29 11826 Daniela Eltrop,
+49 2103 29 11676 e-mail: pr@QIAGEN.com
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