SAN DIEGO, May 27, 2015 /PRNewswire/ -- Halozyme
Therapeutics, Inc. (NASDAQ: HALO) and Ventana Medical Systems, Inc.
(Ventana), a member of the Roche Group, announced today a global
agreement to collaborate on the development of, and for Ventana to
ultimately commercialize, a companion diagnostic assay for use with
Halozyme's investigational new drug, PEGPH20.
The Ventana assay will be used to identify high levels of
hyaluronan (HA). HA is a glycosaminoglycan – a chain of
natural sugars distributed throughout human tissue – that can
accumulate around cancer cells. Halozyme has announced plans for
rollout of a global phase 3 clinical study in 2016 targeting
metastatic pancreatic cancer patients with high HA levels using its
PEGPH20 in combination with ABRAXANE® (nab-paclitaxel)
and gemcitabine.
Under the agreement, Ventana will develop an in vitro
diagnostic (IVD), under design control, using Halozyme's
proprietary HA binding protein, with the intent of submitting it
for regulatory approval in the United
States, Europe and other
countries.
"Ventana brings a high level of development, regulatory and
commercial expertise to our companion diagnostic strategy, which
will help ensure we are well prepared for the initiation of our
phase 3 study in pancreatic cancer," said Dr. Helen Torley, president and CEO of Halozyme.
"The agreement is an important milestone in our PEGPH20 program as
we study the potential of PEGPH20 across multiple tumor types."
"We are pleased to enter into this master collaboration
agreement with Halozyme, which may produce the first diagnostic to
target tumor-associated HA and possibly the first companion
diagnostic assay in pancreatic cancer," said Doug Ward, Vice President, Ventana Companion
Diagnostics. "The PEGPH20 program, coupled with our global reach,
has the potential to improve the standard of care in pancreatic
cancer for patients around the world."
The financial terms of the agreement were not disclosed.
This pharma collaboration is one of many at Ventana, where the
Companion Diagnostics team is developing patient stratifying
diagnostic tools that can help identify those individuals who are
most likely to benefit from specific treatments.
Companion diagnostics (CDx) are tests designed to confirm the
presence of a specific biomarker to assist physicians in selecting
effective therapies for their patients, based on the individual
characteristics of each person. Incorporating a companion
diagnostic strategy into a drug development program may expedite
the drug approval process and help generate more effective
treatments with improved safety profiles for patients.
About Ventana Medical Systems, Inc.
Ventana Medical Systems, Inc. ("VMSI") (SIX: RO, ROG;
OTCQX: RHHBY), a member of the Roche Group, innovates and
manufactures instruments and reagents that automate tissue
processing and slide staining for cancer diagnostics. VENTANA
products are used in clinical histology and drug development
research laboratories worldwide. The company's intuitive,
integrated staining, workflow management platforms, and digital
pathology solutions optimize laboratory efficiencies to help reduce
errors, support diagnosis and enable informed treatment decisions
by anatomic pathology professionals. Together with Roche, VMSI is
driving Personalized Healthcare through accelerated drug
discovery and the development of companion diagnostics to identify
the patients most likely to respond favorably to specific
therapies.
Visit www.ventana.com to learn more.
About PEGPH20
PEGPH20 is an investigational PEGylated form of Halozyme's
proprietary recombinant human hyaluronidase under clinical
development for the systemic treatment of tumors that accumulate
hyaluronan.
The FDA granted orphan drug designation to PEGPH20 for treatment
of pancreatic cancer and fast track for PEGPH20 in combination with
gemcitabine and nab-paclitaxel for the treatment of metastatic
pancreatic cancer. Additionally, the European Commission, acting on
the recommendation from the Committee for Orphan Medicinal Products
of the European Medicines Agency, designated investigational drug
PEGPH20 an orphan medicinal product for the treatment of pancreatic
cancer.
Clinical trials are currently ongoing for development of PEGPH20
in pancreatic ductal adenocarcinoma and in non-small cell lung
cancer. More information may be found at:
http://oncologytrials.halozyme.com/
About Halozyme
Halozyme Therapeutics is a biotechnology company focused on
developing and commercializing novel oncology therapies that target
the tumor microenvironment. Halozyme's lead proprietary program,
our investigational drug PEGPH20, applies a unique approach to
targeting solid tumors, allowing increased access of
co-administered cancer drug therapies to the tumor. PEGPH20
is currently in development for metastatic pancreatic cancer and
non-small cell lung cancer and has potential across additional
cancers in combination with different types of cancer therapies. In
addition to its proprietary product portfolio, Halozyme has
established value-driving partnerships with leading pharmaceutical
companies including Roche, Pfizer, Janssen and Baxter for its drug delivery platform,
ENHANZE™, which enables biologics and small molecule compounds that
are currently administered intravenously to be delivered
subcutaneously. Halozyme is headquartered in San Diego. For
more information visit www.halozyme.com.
Safe Harbor Statement
In addition to historical information, the statements set forth
above include forward-looking statements (including, without
limitation, statements concerning the possible activity, benefits
and attributes of PEGPH20, the possible method of action of
PEGPH20, its potential application to improve cancer therapies and
statements concerning future actions relating to the development of
PEGPH20) that involve risk and uncertainties that could cause
actual results to differ materially from those in the
forward-looking statements. The forward-looking statements are
typically, but not always, identified through use of the words
"believe," "enable," "may," "will," "could," "intends," "estimate,"
"anticipate," "plan," "predict," "probable," "potential,"
"possible," "should," "continue," and other words of similar
meaning. Actual results could differ materially from the
expectations contained in forward-looking statements as a result of
several factors, including unexpected expenditures and costs,
unexpected results or delays in development and regulatory review,
regulatory approval requirements, unexpected adverse events and
competitive conditions. These and other factors that may result in
differences are discussed in greater detail in the Company's
Quarterly Report on Form 10-Q filed with the Securities and
Exchange Commission on May 11,
2015.
CONTACTS:
|
|
|
|
Halozyme
Therapeutics
|
Ventana Medical
Systems
|
Schond
Greenway
|
VMSI Media
Relations
|
858-704-8352
|
Jacqueline
Bucher
|
ir@halozyme.com
|
Vice President,
Marketing &
|
|
Corporate
Communications
|
Jim
Mazzola
|
520-877-7288
o
|
858-704-8122
|
520-468-9145
m
|
ir@halozyme.com
|
jacquie.bucher@ventana.roche.com
|
|
|
|
|
Hyaluronic Acid expressed in pancreatic cancer tissue at 40x
magnification
Logo -
http://photos.prnewswire.com/prnh/20100302/LA63139LOGO
Logo - http://photos.prnewswire.com/prnh/20150527/218705LOGO
Photo - http://photos.prnewswire.com/prnh/20150527/218706
To view the original version on PR Newswire,
visit:http://www.prnewswire.com/news-releases/halozyme-ventana-enter-into-global-agreement-to-collaboratively-develop-companion-diagnostic-for-cancer-treatment-300089204.html
SOURCE Halozyme Therapeutics, Inc.; Ventana Medical Systems,
Inc.