Paralympic Skier Danelle Umstead Teams Up with Spark Therapeutics to Help People Living with Inherited Retinal Diseases (IRDs...
18 Setembro 2019 - 8:30AM
Spark Therapeutics (NASDAQ:ONCE), a fully-integrated, commercial
gene therapy company dedicated to challenging the inevitability of
genetic disease, announced today that it has teamed up with Danelle
Umstead – three-time Paralympian and bronze medalist, 53-time world
cup medalist, “Dancing with the Stars” contestant, wife and mom who
was clinically diagnosed with retinitis pigmentosa (RP), an
inherited retinal disease (IRD) eventually leading to complete
blindness – to encourage people living with IRDs to pursue genetic
testing to uncover the genetic cause of their condition. Danelle is
sharing her personal journey and genetic testing experience as part
of Eye Want 2 Know®, an initiative aimed at helping people living
with IRDs gain more information about their disease through genetic
testing. Spark Therapeutics, committed to increasing information
and knowledge about the diagnosis of a broad range of IRDs, also
recently unveiled an enhanced ID YOUR IRD® gene testing initiative
that tests for variants in approximately 250 genes known to cause
IRDs and includes optional genetic counseling, both available at no
charge subject to the terms and conditions of the program.
At the age of 13, Danelle was clinically diagnosed with RP, a
rare genetic eye condition that involves the breakdown and loss of
cells in the retina eventually leading to complete blindness.
Danelle currently has no central vision and is losing her
peripheral vision.
People living with IRDs have often received a clinical
diagnosis, like choroideremia (CHM), Leber congenital amaurosis
(LCA), cone-rod dystrophy (CRD), retinitis pigmentosa (RP) or
juvenile macular degeneration (JMD), which includes Stargardt
disease. Genetic testing aims to unlock a genetic diagnosis, the
specific gene mutation causing an IRD to progress to complete
blindness. Without a genetic diagnosis, patients, families and
health care professionals can be unprepared to determine the best
disease management plan and evaluate gene-specific clinical trials
or natural history studies.
“Like many people living with RP, an IRD, I was unaware of the
genetic cause of my condition until I pursued genetic testing,”
said Danelle, who is actively training for the next Paralympics.
“With the encouragement of my family and friends, I pursued genetic
testing by using the ’Find a Provider’ tool on the EyeWant2Know.com
website, to locate a health care professional near me to help my
family and me access genetic testing. While I was initially nervous
about getting tested, the process was simple and uncovered the
genetic cause of my condition. The knowledge that I gained through
genetic testing about my specific mutation motivated me to share my
story and become an advocate for genetic testing.”
Danelle urges others living with IRDs to declare “Eye Want 2
Know” and speak with their health care professional about genetic
testing. Patients and families can also access the “Find a
Provider” tool to identify a health care professional nearby to
facilitate genetic testing of IRDs. Health care professionals can
access ID YOUR IRD, a gene testing initiative which is part of Eye
Want 2 Know that tests for variants in approximately 250 genes
known to cause IRDs.
“Danelle’s determination and passion for life, as evidenced by
her athletic accolades and advocacy among the IRD community, makes
her an ideal ambassador for the Eye Want 2 Know initiative
emphasizing the importance of genetic testing,” said, Dan Chung,
D.O., M.A., medical strategy lead, ophthalmology, Spark
Therapeutics. “We urge both patients and families with IRDs to
pursue genetic testing and health care professionals to speak with
their IRD patients about genetic testing.”
Genetic testing may be able to identify the mutated gene
responsible for vision loss. Once a health care professional orders
the ID YOUR IRD test, he or she will collect a saliva or blood
sample from a patient for testing. Results are available in
approximately 14 days from sample receipt by the lab performing the
testing. Armed with this important information, patients can work
with their genetic counselor or health care professional to
determine the best course of action for their disease. Optional
genetic counseling is also available through ID YOUR IRD.
Participation in ID YOUR IRD is subject to the terms and conditions
of the program. Visit EyeWant2Know.com to get started.
About Inherited Retinal Diseases
(IRDs)Inherited retinal diseases (also known as inherited
retinal dystrophies, or IRDs) are a group of rare eye disorders
caused by various inherited gene mutations and can result in
progressive vision loss or total blindness. Common IRDs include
choroideremia (CHM), Leber congenital amaurosis (LCA), cone-rod
dystrophy (CRD), retinitis pigmentosa (RP) and juvenile macular
degeneration (JMD), which includes Stargardt disease.
About Spark Therapeutics At Spark
Therapeutics, a fully integrated, commercial company committed to
discovering, developing and delivering gene therapies, we
challenge the inevitability of genetic
diseases, including blindness, hemophilia, lysosomal
storage disorders and neurodegenerative diseases. We currently
have four programs in clinical trials. At Spark, we see the
path to a world where no life is limited by genetic disease. For
more information, visit www.sparktx.com, and follow us
on Twitter and LinkedIn.
CAUTIONARY STATEMENT REGARDING FORWARD-LOOKING
STATEMENTS This release contains "forward-looking
statements" within the meaning of the Private Securities Litigation
Reform Act of 1995, including statements regarding the company's
Eye Want 2 Know program. The words ‘‘anticipate,’’ ‘‘believe,’’
‘‘expect,’’ ‘‘intend,’’ ‘‘may,’’ ‘‘plan,’’ ‘‘predict,’’ ‘‘will,’’
‘‘would,’’ ‘‘could,’’ ‘‘should,’’ ‘‘continue’’ and similar
expressions are intended to identify forward-looking statements,
although not all forward-looking statements contain these
identifying words. We may not actually achieve the plans,
intentions or expectations disclosed in our forward-looking
statements, and you should not place undue reliance on our
forward-looking statements. Any 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, but are not limited to, the risk
that: (i) Eye Want 2 Know does not ensure the IRD community is
aware of and appreciates the urgency for genetic testing, (ii) the
critical barriers to adopting genetic testing are different than
what we believe, and (iii) genetic testing, including ID YOUR IRD,
may not provide clarity, accuracy, resources or community support
to those living with an IRD. For a discussion of other risks and
uncertainties, and other important factors, any of which could
cause our actual results to differ from those contained in the
forward-looking statements, see the "Risk Factors" section, as well
as discussions of potential risks, uncertainties and other
important factors, in our Annual Report on Form 10-K, as amended,
our Quarterly Reports on Form 10-Q and other filings we make with
the U.S. Securities and Exchange Commission. All information
in this press release is as of the date of the release, and Spark
undertakes no duty to update this information unless required by
law.
Investor Relations Contact: |
Media
Contact: |
Ryan Asay |
Kevin Giordano |
Ryan.asay@sparktx.com |
Kevin.giordano@sparktx.com |
(215) 239-6424 |
(215) 294-9942 |
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