Foundation Medicine and Pfizer Announce Broad Partnership to Develop Companion Diagnostics for Pfizer’s Oncology Portfolio
January 16 2018 - 7:00AM
Business Wire
-- Foundation Medicine’s Data Analytics
Platform Will Assist Pfizer in Advancing Discovery and Clinical
Development of Novel Oncology Therapies --
Foundation Medicine, Inc. (NASDAQ:FMI) today announced that the
company has entered into a broad partnership with Pfizer Inc.
(NYSE: PFE). The partnership focuses on development, regulatory
support and commercialization of companion diagnostics (CDx) that
will be included in updates to FoundationOne CDx™. FoundationOne
CDx is Foundation Medicine’s FDA-approved comprehensive genomic
profiling (CGP) assay for all solid tumors that incorporates
multiple companion diagnostics. Pfizer will also benefit from
access to FoundationInsights™, Foundation Medicine’s data analytics
platform, to facilitate novel biomarker discovery and to optimize
clinical trial design. The unique combination of
FoundationInsights™ and FoundationOne CDx will potentially enable
Pfizer to leverage Foundation Medicine’s platform technology to
accelerate discovery and development of precision oncology
therapeutics.
Pfizer currently has 10 FDA-approved oncology medicines that
treat a diverse array of solid tumors and hematologic malignancies.
In addition, its oncology pipeline includes 17 assets in clinical
development and 19 phase 3 studies.
“Our mission to transform cancer care includes partnering with
biopharma companies to expedite development of personalized
treatment options for patients. We are proud to partner with Pfizer
who shares our commitment to precision oncology and
biomarker-driven drug development,” said Melanie Nallicheri, chief
business officer and head of biopharma at Foundation Medicine. “The
combination of our FDA-approved comprehensive genomic profiling
platform and molecular information solutions, coupled with Pfizer’s
robust oncology portfolio, enables us to enhance the impact of
precision oncology to advance patient care.”
FoundationOne CDx assesses all classes of genomic alterations in
324 genes known to drive cancer growth, providing potentially
actionable information to help guide treatment decisions. It also
reports genomic biomarkers, such as microsatellite instability
(MSI) and tumor mutational burden (TMB), that can help inform the
use of immunotherapies; genomic alterations in other genes relevant
to patient management; and relevant clinical trial information. As
such, it is designed to help streamline companion diagnostic
development, mitigate risk and advance targeted therapy
development. Currently FoundationOne CDx is FDA-approved as a CGP
assay for all solid tumors and a broad companion diagnostic for
patients with certain types of non-small cell lung cancer,
melanoma, colorectal cancer, ovarian cancer or breast cancer to
identify those patients who may benefit from treatment with one of
17 on-label targeted therapies.
Concurrent with FDA approval, the Centers for Medicare &
Medicaid Services (CMS) issued a preliminary National Coverage
Determination (NCD) for FoundationOne CDx. The draft NCD would
provide coverage for FDA-approved companion diagnostic claims, as
well as a pathway for additional coverage with evidence development
in other solid tumor types. The final policy is expected to issue
during the first quarter of 2018 following public comment on the
preliminary NCD and an administrative period.
About FoundationOne CDxFoundationOne CDx is a next
generation sequencing based in vitro diagnostic device for
detection of substitutions, insertion and deletion alterations
(indels), and copy number alterations (CNAs) in 324 genes and
select gene rearrangements, as well as genomic signatures including
microsatellite instability (MSI) and tumor mutational burden (TMB)
using DNA isolated from formalin-fixed paraffin embedded (FFPE)
tumor tissue specimens. FoundationOne CDx is intended as a
companion diagnostic to identify patients who may benefit from
treatment with certain targeted therapies in accordance with their
approved therapeutic product labeling. Additionally, FoundationOne
CDx is intended to provide tumor mutation profiling to be used by
qualified health care professionals in accordance with professional
guidelines in oncology for patients with solid malignant neoplasms.
For a full list of targeted therapies for which FoundationOne CDx
is indicated as a companion diagnostic, please visit
http://www.foundationmedicine.com/genomic-testing/foundation-one-cdx.
About Foundation MedicineFoundation Medicine (NASDAQ:FMI)
is a molecular information company dedicated to a transformation in
cancer care in which treatment is informed by a deep understanding
of the genomic changes that contribute to each patient's unique
cancer. The company offers a full suite of comprehensive genomic
profiling assays to identify the molecular alterations in a
patient's cancer and match them with relevant targeted therapies,
immunotherapies and clinical trials. Foundation Medicine’s
molecular information platform aims to improve day-to-day care for
patients by serving the needs of clinicians, academic researchers
and drug developers to help advance the science of molecular
medicine in cancer. For more information, please visit
http://www.FoundationMedicine.com or follow Foundation Medicine on
Twitter (@FoundationATCG).
Foundation Medicine® is a registered trademark, and
FoundationOne CDx™ and FoundationInsights™ are trademarks of
Foundation Medicine, Inc.
Cautionary Note Regarding Forward-Looking Statements for
Foundation MedicineThis press release contains "forward-looking
statements" within the meaning of the Private Securities Litigation
Reform Act of 1995, including, but not limited to, statements
regarding a collaboration
between Pfizer and Foundation Medicine; the ability
of Foundation Medicine products and services, including
FoundationOne CDx, to accelerate drug discovery and development;
and the timing or scope of any NCD issued by CMS. All such
forward-looking statements are based on management's current
expectations of future events and are subject to a number of risks
and uncertainties that could cause actual results to differ
materially and adversely from those set forth in or implied by such
forward-looking statements. These risks and uncertainties include
the risks that the collaboration does not proceed as expected or
does not meet the objectives of the parties; a delay on the part
of, or failure of, CMS to issue a final NCD; and the risks
described under the caption "Risk Factors" in Foundation
Medicine's Annual Report on Form 10-K for the year
ended December 31, 2016, filed with the Securities and
Exchange Commission on March 2, 2017, as well as other
risks detailed in Foundation Medicine's subsequent
filings with the Securities and Exchange Commission. All
information in this press release is as of the date of the release,
and Foundation Medicine undertakes no duty to update this
information unless required by law.
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version on businesswire.com: http://www.businesswire.com/news/home/20180116005430/en/
Foundation Medicine, Inc.Media Contact:Lee-Ann Murphy,
617-245-3077pr@foundationmedicine.comorInvestor
Contact:Kimberly Brown,
617-418-2215ir@foundationmedicine.com
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