Natera, Inc. - NTRA STOCK NEWS

Natera, Inc. (NASDAQ: NTRA) presented key findings at the 2021 San Antonio Breast Cancer Symposium highlighting the use of its Signatera test in high-risk breast cancer patients. The studies indicated that detecting circulating tumor DNA (ctDNA) both pre- and post-surgery was crucial in predicting disease relapse, with ctDNA status being the strongest predictor of patient outcomes. As a custom-built test for monitoring cancer treatment, Signatera has shown significant potential in clinical settings for improving patient care and optimizing treatment strategies.

Natera, Inc. (NASDAQ: NTRA) announced the acceptance of the first manuscript from its groundbreaking SMART study for publication in the American Journal of Obstetrics and Gynecology. This study validates the Panorama non-invasive prenatal test (NIPT) for common trisomies, confirming its 99% sensitivity and >99.5% specificity for trisomy 21. The SMART study, involving over 20,000 patients, utilized an advanced AI algorithm, Panorama AI, which lowered the no-call rate to 1.5%. This research enhances the confidence of physicians in screening for genetic disorders during pregnancy.

Natera announced that the CMS has issued a final local coverage determination for pan-cancer immunotherapy monitoring using its Signatera molecular residual disease test. This coverage applies to Medicare patients undergoing immunotherapy, significantly expanding access to personalized monitoring. The Signatera test has shown high predictive accuracy in identifying non-responders early in treatment, aiming to improve cancer care outcomes. Natera sees this development as a crucial step in enhancing treatment decisions across various tumor types.

Natera, Inc. (NASDAQ: NTRA) reported a strong third quarter for 2021, achieving $158.1 million in total revenues, a 61.1% increase year-over-year. Product revenues rose to $150.7 million, driven by a 55.4% increase in processed tests, totaling 407,300. Despite a net loss of $151.3 million or ($1.63) per diluted share, the company raised its 2021 revenue guidance to $615-$625 million. Significant advancements include an exclusive biobank license and positive results from the Trifecta Study in kidney transplant.

Natera, Inc. (NASDAQ: NTRA) announced initial results from the Trifecta study, the largest biopsy-matched evaluation of donor-derived cell-free DNA (dd-cfDNA) in kidney transplant recipients. The study analyzed over 300 biopsy-matched samples, revealing that the Prospera test with quantification demonstrated an AUC of 0.81 for rejection detection, improving to 0.91 when differentiating rejection from quiescence. Natera anticipates publishing comprehensive results in early 2022, reinforcing its leadership in cfDNA technology.

Natera, Inc. (NASDAQ: NTRA) will announce its third-quarter 2021 financial results on November 4, 2021, after market close. A conference call to discuss these results, along with business activities and financial outlook, will take place at 1:30 p.m. PT (4:30 p.m. ET). Investors can join the call via live dial-in or webcast, with options for domestic and international participants. A replay of the webcast will be available later at investor.natera.com.

Natera, Inc. (NASDAQ: NTRA) has launched the Prospera Lung test, expanding its organ health offerings to include lung transplant assessments. Validated in the VALID study, this non-invasive test achieves a negative predictive value of 97.33% and 89.06% sensitivity, distinguishing between stable patients and acute rejection effectively. Natera also announced two new studies to compare Prospera against traditional biopsy methods. The company aims to improve patient outcomes among lung transplant recipients, addressing a significant clinical need for accurate monitoring.

Natera, Inc. (NASDAQ: NTRA) announced a new study published in Clinical Cancer Research validating its Signatera test for assessing tumor growth rates and predicting survival in early-stage colorectal cancer. This multi-center study involved 168 patients and demonstrated that MRD-positive patients can be stratified based on circulating tumor DNA (ctDNA) growth rates. Key findings included a 9.8-month lead time for recurrence detection and the association of ctDNA clearance with improved survival outcomes, showcasing the value of personalized ctDNA analysis in clinical decision-making.