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Natera, Inc. (Symbol: NTRA) is a leading diagnostic and research company based in San Carlos, CA, driven by a commitment to advance the science and application of prenatal testing. In the information age, medical diagnostics have lagged behind in adopting new technologies, but Natera is changing that narrative. The company specializes in preconception and prenatal genetic testing services, providing couples with crucial information throughout the pregnancy journey.
Natera offers a comprehensive range of tests, including Preimplantation Genetic Diagnosis (PGD) for IVF and Non-Invasive Prenatal Testing (NIPT). Their Panorama NIPT is particularly notable for its ability to screen for chromosomal abnormalities in a fetus, even in twin pregnancies, typically through a simple blood draw from the mother. Another significant product is the Horizon Carrier Screening (HCS), which determines carrier status for numerous severe genetic diseases that could be passed on to offspring.
The company's innovative approach leverages advances from the Human Genome Project and is powered by proprietary bioinformatics algorithms. This technology enables highly accurate genetic testing results. Natera's portfolio also includes the Signatera Molecular Residual Disease (MRD) Test, designed to detect circulating tumor DNA in cancer patients, helping to assess molecular residual disease and monitor recurrence. Additionally, the Prospera test assesses organ transplant rejection.
Through its pioneering genetic testing services and experienced genetic counseling, Natera provides valuable insights that help in informed decision-making for pregnancies and medical conditions. The company continues to make significant strides in the field of medical diagnostics, driven by a passion for innovation and excellence.
Natera, Inc. (NASDAQ: NTRA) has published a new paper in Pediatric Nephrology showcasing the clinical utility of its Renasight™ test for kidney disease diagnosis. The case study details a 16-year-old patient with sickle cell disease who was identified with autosomal dominant polycystic kidney disease (ADPKD) through genetic testing. This revelation emphasizes the importance of broad-panel genetic testing in managing patients with dual genetic conditions. Natera is conducting a prospective study, RenaCARE, across over 30 sites in the U.S. to further establish the test's clinical benefits.
Natera, Inc. (NASDAQ: NTRA) has announced new data on its personalized molecular residual disease (MRD) test, Signatera, set to be presented at the ASCO GI 2023 from January 19-21 in San Francisco. The presentations will showcase Signatera's effectiveness in assessing MRD across various gastrointestinal cancers, including colorectal and anal cancers. Notably, a study involving 14,425 patients suggests that MRD testing could commence as early as 2 weeks post-surgery, maintaining test sensitivity. This supports Signatera’s role in personalized cancer treatment. For further details, visit Natera’s website.
Natera, Inc. (NASDAQ: NTRA) has published a new study in Nature Medicine, highlighting the efficacy of the SignateraTM molecular residual disease (MRD) test for identifying patients with stage II-IV colorectal cancer at risk of recurrence. Data from the GALAXY arm of the CIRCULATE-Japan trial revealed that MRD-positive patients (18%) significantly benefited from adjuvant chemotherapy (ACT), while MRD-negative patients (82%) did not. The study also confirmed a pre-surgical detection rate of 95.9% for stage II-III patients, emphasizing the predictive power of Signatera in treatment decisions. This evidence builds on prior findings at ASCO GI 2022.
Natera, Inc. (NASDAQ: NTRA) announced it will present at the 41st Annual J.P. Morgan Healthcare Conference on January 10, 2023, at 9:45 a.m. PT (12:45 p.m. ET). Natera's management will deliver a presentation and host a Q&A session with investors. The presentation can be accessed via a live webcast on Natera's Investor Relations website, where it will also be archived for later viewing. Natera is a leader in cell-free DNA testing focused on oncology, women's health, and organ health, with a commitment to advancing personalized genetic testing.
Natera, Inc. (NASDAQ: NTRA) supports the updated guidelines from the International Society for Heart and Lung Transplantation, which recommends donor-derived cfDNA testing for heart transplant surveillance. The new guidelines advocate monthly rejection monitoring for the first six months post-transplant and again at nine and twelve months. Natera's Prospera™ Heart dd-cfDNA test, launched in late 2021, identifies allograft rejection non-invasively. The test has shown clinical validation in studies, enhancing care for heart transplant patients.
Natera, Inc. (NASDAQ: NTRA) announced a study published in JCO Precision Oncology on its ctDNA test, Signatera™, for predicting recurrence in esophageal and gastric cancers (EGCs). The real-world study involved 295 patients and 943 plasma samples. Key findings showed that pre-operative ctDNA was detectable in 96% of patients, while 23.5% post-surgery showed ctDNA presence, correlating with an 81.2% recurrence rate. Signatera proved to be the strongest prognostic factor compared to other clinicopathological factors. This underscores the test's role in better risk stratification and management of EGCs.
Natera, Inc. (NASDAQ: NTRA) will present new data at the 2022 San Antonio Breast Cancer Symposium in San Antonio, Texas, focusing on its Signatera and Empower tests. The presentations will include findings from the LEADER and I-SPY 2 clinical trials concerning breast cancer recurrence monitoring and hereditary cancer risk management. Notable highlights include two posters on December 8 and 9, showcasing the effectiveness of personalized circulating-tumor DNA testing and cell-free DNA monitoring in breast cancer management. Natera aims to provide insights for improved patient care.
Natera has published a clinical experience study showcasing its Panorama SNP-based noninvasive prenatal test (NIPT) for twin pregnancies, with findings based on 18,984 cases over 27 months. The study demonstrated a positive predictive value (PPV) of 88.7% for trisomy 21 screening, reaching 90.4% when including suggestive findings. Unique to Panorama is its ability to determine zygosity. The study corroborates earlier findings that aneuploidy rates are higher in dizygotic twins. Natera emphasizes its commitment to generating real-world evidence to enhance prenatal care.
Natera, Inc. (NASDAQ: NTRA), a leader in cell-free DNA testing, will participate in the Piper Sandler 34th Annual Healthcare Conference on November 30, 2022, at 12:00 p.m. PT (3:00 p.m. ET). CEO Steve Chapman and CFO Mike Brophy will present at the event held at the Lotte New York Palace. A live webcast of the presentation will be accessible on the Natera Investor Relations website and archived for future reference.
Natera, Inc. (Nasdaq: NTRA) announced the pricing of its underwritten public offering of 11,430,000 shares of common stock at $35.00 per share. The offering is expected to close on November 18, 2022, subject to customary conditions. Additionally, Natera has granted underwriters a 30-day option to purchase up to 1,714,500 additional shares. Morgan Stanley, Cowen, and SVB Securities are managing the offering, which is filed under an effective shelf registration statement with the SEC. This issuance aims to support Natera's ongoing operations in cell-free DNA testing for oncology and women's health.