-- Expanded offering now one of the most comprehensive and includes
testing for endocrine, blood, bone, brain, genitourinary, sarcoma, and
skin cancers --
SAN FRANCISCO--(BUSINESS WIRE)--
Invitae
Corporation (NYSE:NVTA),
a genetic information company, today announced that it has expanded its hereditary
cancer genetic testing menu, now offering an even more comprehensive
testing menu that covers all major hereditary cancers.
Invitae has expanded its test menu to include blood, bone, brain,
endocrine (hyperparathyroidism, thyroid cancer, and
paraganglioma-pheochromocytoma), genitourinary (renal/urinary tract and
prostate cancer), sarcoma, and skin cancers (melanoma and basal cell
nevus syndrome). This expanded test menu is offered at the same price
and with the same flexibility as all of Invitae’s genetic tests.
“A broad hereditary cancer testing menu provides clinicians with
options, to choose a single or a set of genes. Providers have therefore
a flexibility to test for a single specific syndrome, or since many
clinical scenarios overlap between many syndromes, then the clinician
can ask for a wider panel with synchronous testing,” said Fadi Braiteh
MD, Director of the Phase I oncology program and GI malignancies program
for Comprehensive
Cancer Centers of Nevada. “The availability and ease of ordering,
the robustness of the technology and quality assurance, coupled with a
conscious effort for cost-saving are essential, and should be on the
mind of each clinician. These new panels provide us with such an option.”
In addition, Invitae is introducing three new, focused panels based
entirely on oncology management guidelines in breast, gynecologic, and
colon cancer. Invitae is also pleased to offer epidermal growth factor
receptor (EGFR) testing for patients with strong personal and family
history of lung cancer, particularly when there is no history of
environmental exposures such as tobacco smoking or radon.
“Invitae is committed to providing genetic testing in the most
medically-responsible way. Often management guidelines for hereditary
cancer genetic testing dictate how surgeons and oncologists treat their
patients,” said Robert Nussbaum, MD, chief medical officer of Invitae.
“With responsible, guidelines-based medical practice and Invitae’s
expanded cancer menu, clinicians are able to provide patients and
providers with testing that is relevant to the diagnosis of an even
greater number of hereditary cancer syndromes.”
Invitae offers a transparent pricing structure independent of the number
of genes required to provide an accurate diagnosis for any specific
clinical indication. For payers and institutions that are in contract
with Invitae, the price per indication can be as low as $950, depending
on the payer’s requirements. For third-party payers with whom Invitae is
out-of-network and for non-contracted institutions, the price per
indication is $1,500. In addition, for patients without third-party
insurance coverage or who do not meet insurance criteria for coverage,
Invitae offers its full test menu for $475 per indication for patients
whose clinician has ordered the testing online and who register online
and pay in advance for the testing.
About Invitae
Invitae Corporation's (NYSE:NVTA) mission is to bring comprehensive
genetic information into mainstream medical practice to improve the
quality of healthcare for billions of people. Invitae’s goal is to
aggregate most of the world’s genetic tests into a single service with
higher quality, faster turnaround time, and lower price than many
single-gene and panel tests today. The company currently provides a
single diagnostic service comprising hundreds of genes for a variety of
genetic disorders associated with oncology, cardiology, neurology,
pediatrics and other rare disease areas.
For more information, visit our website at ir.invitae.com
and follow us on Twitter: @invitae
and @invitaeIR.
Safe Harbor Statements
This press release contains forward-looking statements within the
meaning of the Private Securities Litigation Reform Act of 1995,
including statements relating to the company’s belief that it can
accelerate the adoption of comprehensive genetic information into
mainstream medical care and realize its mission; the timing of any new
testing service releases and the attributes of any such services; the
company’s beliefs regarding the benefits of its pricing program; the
company’s belief that its expanded cancer menu will help clinicians be
able to provide patients and providers with testing that is relevant to
diagnoses; the company’s beliefs with respect to the availability of
EGFR testing; the attributes and benefits of the company’s tests to
patients, physicians and payers; and the indicators of the company’s
success and its expected actions with respect to those indicators.
Forward-looking statements are subject to risks and uncertainties that
could cause actual results to differ materially, and reported results
should not be considered as an indication of future performance. These
risks and uncertainties include, but are not limited to: the company’s
history of losses; the company’s need to scale its infrastructure in
advance of demand for its tests and to increase demand for its tests;
the company’s ability to develop and commercialize new tests and expand
into new markets; the risk that the company may not obtain or maintain
sufficient levels of reimbursement for its tests; risks associated with
the company’s ability to use rapidly changing genetic data to interpret
test results accurately and consistently; the company’s ability to
compete; laws and regulations applicable to the company’s business,
including potential regulation by the Food and Drug Administration; and
the other risks set forth in the company’s filings with the Securities
and Exchange Commission, including the risks set forth in the company’s
Quarterly Report on Form 10-Q for the quarter ended September 30, 2015.
These forward-looking statements speak only as of the date hereof, and
Invitae Corporation disclaims any obligation to update these
forward-looking statements.
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Source: Invitae Corporation