Full Press Release Details
Announces Development and Co-Marketing Agreement with Thermo Fisher Scientific to Expand Access to Precision Oncology
extends global reach for Thermo Fisher's rapid next-generation sequencing technology
Calif., January 18, 2022 - Oncocyte Corporation (Nasdaq: OCX), a precision diagnostics company with the mission to improve
patient outcomes by providing clear insights that inform critical decisions in the diagnosis, treatment, and monitoring of cancer, today
announced a development and co-marketing agreement for two distributed in vitro diagnostic (IVD) assays on Thermo Fisher Scientific's
Ion TorrentTM GenexusTM System.* The agreement also grants Oncocyte rights to develop future companion diagnostics
on the Genexus System.
the terms of the collaboration, Oncocyte will clinically validate Thermo Fisher's existing Oncomine Comprehensive Assay Plus* on
the Genexus System paving the way toward IVD clearance for use in tumor profiling and future submissions as
a companion diagnostic. As an IVD, the >500-gene assay will initially be able to provide physicians with information about
patients' tumors in accordance with clinical evidence, applicable clinical trials, and future approval may assist with the
selection of targeted therapies. Oncocyte will also develop its 27-gene expression DetermaIOTM test as a distributed kit on
the Genexus. DetermaIO may predict response to immuno-oncology therapies based on data demonstrating potential pan-cancer utility and
improvement over current standard-of-care tests.
many as 44% of newly diagnosed cancer patients may be eligible for immuno-oncology therapies, with additional patients potentially benefitting
from other precision medicines, yet many patients' tumors are never sequenced to determine if they may benefit from these targeted
treatments,1" said Ron Andrews, President and Chief Executive Officer of Oncocyte. "In order to increase the number
of patients benefiting from precision medicine, we need to expand the number of IVDs and develop these tests on instruments that are
designed to make sequencing-based testing simple and more accessible. We have developed our Determa menu to ultimately become regulated
kits for distribution ex-US on an IVD instrument. Our collaboration with Thermo Fisher using the Genexus System's end-to-end
automation enables that vision."
Andrews continued, "Leveraging Thermo Fisher's proven global capabilities and installed base will enable us to expand the
availability of IVD assays beyond the U.S. market. The collaboration with Thermo Fisher, along with the resulting IVD test kits and potential
companion diagnostic tests that we will seek to develop and market together, will play a key role in helping us improve patient outcomes
first-of-its-kind Genexus System is designed to be used in any lab and delivers comprehensive next-generation sequencing (NGS) results
in as little as a single day - the same timeframe as single-gene tests, such as immunohistochemistry (IHC) assays. The Genexus
system's flexible batching makes it an attractive solution for hospital labs with low and medium testing volume by reducing the
need to wait several days until a lab has a sufficient number of samples to test. The integrated purification system and sequencer enable
sample preparation and processing with only 20 minutes of hands-on time and minimal user intervention, allowing for the democratization
of NGS to community and regional cancer centers globally.
testing can have a dramatic impact on patient care, especially when results are available quickly to support early clinical decision-making,"
said Garret Hampton, President, clinical next-generation sequencing and oncology at Thermo Fisher Scientific. "Today, access to
comprehensive testing depends on where you are treated. Our goal is to democratize genomic profiling so it is available to patients right
away in more clinical settings - ultimately, everywhere patients receive treatment. By partnering with Oncocyte to validate
and co-develop new IVD assays, we are working to expand access to genomic profiling and spread the benefits of precision medicine to
for Research Use Only. Not for use in diagnostic procedures.
Haslam and Prasad. (2019) Estimation of the percentage of US patients with cancer who are eligible for and respond to checkpoint
inhibitor immunotherapy drugs. JAMA Network Open 2(5):e192535.
is a precision diagnostics and monitoring company with the mission to improve patient outcomes by providing clear insights that inform
critical decisions in the diagnosis, treatment, and monitoring of cancer. The Company, through its proprietary tests and pharmaceutical
services business, aims to help save lives by accelerating the diagnosis of cancer and advancing cancer care. The Company's tests
are designed to help provide clarity and confidence to physicians and their patients at every stage. DetermaRx identifies early-stage
lung cancer patients who are at high risk for cancer recurrence and who may benefit from adjuvant chemotherapy. DetermaIO , a gene
expression test currently used as a research-use only tool, assesses the tumor microenvironment to predict response to immunotherapies.
The Company's pipeline of tests in development also includes DetermaTx , which will assess mutational status of a tumor,
blood-based monitoring test DetermaCNI , and long-term recurrence monitoring test DetermaMx . In addition, Oncocyte's
pharmaceutical services provide companies that are developing new cancer treatments a full suite of molecular testing services to support
the drug development process.
DetermaIO , DetermaTx , DetermaCNI , DetermaMx and TheraSure are trademarks of Oncocyte Corporation.
Forward Looking Statements
cautions you that this press release contains forward-looking statements. Any statements that are not historical fact (including, but
not limited to statements that contain words such as "will," "believes," "plans," "anticipates,"
"expects," "estimates," "may," and similar expressions) are forward-looking statements. These statements
include those pertaining to, among other things, the transactions contemplated by the development and co-marketing agreement for two
distributed in vitro diagnostic (IVD) assays on Thermo Fisher Scientific's Ion TorrentTM GenexusTM System, the expectations to
clinically validate Thermo Fisher's existing Oncomine Comprehensive Assay Plus* on the Genexus System paving the way toward in
vitro diagnostic (IVD) clearance for use in tumor profiling and the potential for future development of companion diagnostic applications, the ability to provide physicians with information about patients' tumors in accordance with clinical
evidence, applicable clinical trials, and assist with the selection of targeted therapies, the development of Oncocyte's 27-gene
expression DetermaIOTM test as a distributed kit on the Genexus, the ability to predict responses to immuno-oncology therapies based
on data demonstrating potential pan-cancer utility and improvement over current standard-of-care tests, the expansion of IVD assays beyond
the U.S. market and improve patient outcomes worldwide, the ability to democratize genomic profiling so it is available to patients right
away in more clinical settings, and other statements about the future expectations, beliefs, goals, plans, or prospects expressed by
management. Forward-looking statements involve risks and uncertainties, including, without limitation, the potential impact of COVID-19
on Oncocyte or its subsidiaries' financial and operational results, risks inherent in the development and/or commercialization
of diagnostic tests or products, uncertainty in the results of clinical trials or regulatory approvals, the capacity of Oncocyte's
third-party supplied blood sample analytic system to provide consistent and precise analytic results on a commercial scale, potential
interruptions to supply chains, the need and ability to obtain future capital, maintenance of intellectual property rights in all applicable
jurisdictions, obligations to third parties with respect to licensed or acquired technology and products, the need to obtain third party
reimbursement for patients' use of any diagnostic tests Oncocyte or its subsidiaries commercialize in applicable jurisdictions,
and risks inherent in strategic transactions such as the potential failure to realize anticipated benefits, legal, regulatory or political
changes in the applicable jurisdictions, accounting and quality controls, potential greater than estimated allocations of resources to
develop and commercialize technologies, or potential failure to maintain any laboratory accreditation or certification. Actual results
may differ materially from the results anticipated in these forward-looking statements and accordingly such statements should be evaluated
together with the many uncertainties that affect the business of Oncocyte, particularly those mentioned in the "Risk Factors"
and other cautionary statements found in Oncocyte's Securities and Exchange Commission (SEC) filings, which are available from
the SEC's website. You are cautioned not to place undue reliance on forward-looking statements, which speak only as of the date
on which they were made. Oncocyte undertakes no obligation to update such statements to reflect events that occur or circumstances that
exist after the date on which they were made, except as required by law.
LifeSci Advisors, LLC
Westwicke Healthcare PR