Natera Announces National Commercial Coverage for its Fetal RhD NIPT
03 2월 2025 - 9:00PM
Business Wire
Coverage from one of the largest payors in the
country expands access to fetal RhD testing for pregnant patients
nationwide
Natera, Inc. (NASDAQ: NTRA), a global leader in cell-free DNA
(cfDNA) and genetic testing, today announced a new policy for
commercial coverage of its cfDNA Fetal RhD noninvasive prenatal
test (Fetal RhD NIPT) from one of the largest payors in the United
States.
Effective as of Jan. 2025, the policy notes that coverage of
fetal RhD testing is available when a pregnancy may be at risk for
alloimmunization, when paternal antigen typing is unavailable or
heterozygous, and if a patient declines amniocentesis or it is not
recommended for the pregnancy.
Up to 15 percent of pregnant patients are RhD-negative1. When
the maternal blood type is RhD-negative and the fetal blood type is
RhD-positive, antibodies can develop (alloimmunization) that can
lead to hemolytic disease of the fetus and newborn.
Natera’s Fetal RhD NIPT can be performed as early as nine weeks
gestation and determines fetal RhD status from the blood of a
pregnant patient. It is offered through the Company’s women’s
health suite of products, which includes Panorama, the no. 1
ordered NIPT in the U.S.
“These new policies expand access to important testing that can
prevent unnecessary medical treatment in pregnancies,” said Ramesh
Hariharan, PhD, General Manager of Women’s Health at Natera.
“Broadening commercial coverage to include fetal RhD testing
reinforces the importance of this offering and the benefits it can
bring to pregnant patients nationwide.”
About Natera
Natera™ is a global leader in cell-free DNA and genetic testing,
dedicated to oncology, women’s health, and organ health. We aim to
make personalized genetic testing and diagnostics part of the
standard of care to protect health and inform earlier, more
targeted interventions that help lead to longer, healthier lives.
Natera’s tests are validated by more than 250 peer-reviewed
publications that demonstrate high accuracy. Natera operates ISO
13485-certified and CAP-accredited laboratories certified under the
Clinical Laboratory Improvement Amendments (CLIA) in Austin, Texas,
and San Carlos, California. For more information, visit
www.natera.com.
Forward-Looking Statements
All statements other than statements of historical facts
contained in this press release are forward-looking statements and
are not a representation that Natera’s plans, estimates, or
expectations will be achieved. These forward-looking statements
represent Natera’s expectations as of the date of this press
release, and Natera disclaims any obligation to update the
forward-looking statements. These forward-looking statements are
subject to known and unknown risks and uncertainties that may cause
actual results to differ materially, including with respect to
coverage and reimbursement determinations from third-party payers,
or our expectations of the benefits of our tests and product
offerings to patients, providers and payers. Additional risks and
uncertainties are discussed in greater detail in "Risk Factors" in
Natera’s recent filings on Forms 10-K and 10-Q, and in other
filings Natera makes with the SEC from time to time. These
documents are available at www.natera.com/investors and
www.sec.gov.
References
1. Zipursky A, Paul VK. The global burden of Rh disease. Arch
Dis Child Fetal Neonatal Ed 2011;96:F84–5. (Level III)
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version on businesswire.com: https://www.businesswire.com/news/home/20250203957122/en/
Investor Relations: Mike Brophy, CFO, Natera, Inc.,
510-826-2350, investor@natera.com Media: Lesley Bogdanow, VP of
Corporate Communications, Natera, Inc., pr@natera.com
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