^
Contact us  to learn more about
our Premium Content:  News alerts, weekly reports and conference planners

COMPANY:
Natera

i
Other names: Natera | Natera Inc | Natera Inc. | Natera, Inc. | Gene Security Network | Gene Security Network Inc | Gene Security Network Inc. | Gene Security Network, Inc.
Related tests:
Evidence

News

7d
New Signatera™ Data in Lymphoma and Multiple Myeloma to be Presented at the 2025 American Society of Hematology Annual Meeting (Natera Press Release)
"Natera...announced that new data on Signatera will be presented at the 2025 American Society of Hematology (ASH) Annual Meeting, taking place December 6-9, 2025, in Orlando, Florida. Natera and its collaborators will present four abstracts highlighting the clinical validity and utility of Signatera in hematologic malignancies."
Clinical data
|
Signatera™
8d
Natera to Present 12 Datasets Including >50,000 Patients Featuring Signatera™ at the San Antonio Breast Cancer Symposium (Natera Press Release)
"Natera, Inc...today announced that at least twelve abstracts highlighting Signatera will be shared at the 2025 San Antonio Breast Cancer Symposium (SABCS)"
Clinical data
|
Signatera™
8d
NSABP FC-13 (EMPIRE): A phase II platform study of cemiplimab monotherapy or cemiplimab-based combinations in patients with colorectal cancer and minimal residual disease (MRD) after definitive therapy. (ASCO-GI 2026)
P2 | "Funded by Regeneron, Natera, Inc., NSABP Foundation, Inc. Clinical Trial Registration Number: NCT07058012 The full, final text of this abstract will be available on Jan 05 at 05:00 PM EST."
Clinical • P2 data • Minimal residual disease
|
Libtayo (cemiplimab-rwlc)
8d
NRG-GI008: Colon adjuvant chemotherapy based on evaluation of residual disease (CIRCULATE-North America). (ASCO-GI 2026)
P2/3 | "Funded by U.S. National Institutes of Health, U.S. National Institutes of Health, U.S. National Institutes of Health, U.S. National Institutes of Health, Natera, Inc. Clinical Trial Registration Number: NCT05174169 The full, final text of this abstract will be available on Jan 05 at 05:00 PM EST."
Clinical
1m
Natera Announces Expansion to 20 Genes for its Fetal Focus™ Single-Gene NIPT (Natera Press Release)
" Natera...today announced it will expand its Fetal Focus test to cover 20 genes, marking a major advancement in single-gene noninvasive prenatal testing (sgNIPT). Building on the success of the initial Fetal Focus 5-gene test, launched in August, the new expanded panel will launch in Q4 2025."
Clinical
1m
Natera Reports Strong Advanced Adenoma Data from Prospective PROCEED-CRC Trial, Demonstrating 22.5% Sensitivity and 91.5% Specificity (Natera Press Release)
"Natera...today announced another successful readout for its ECD program, which is evaluating a blood-based screening test for the detection of CRC and advanced adenomas (AA). This latest analysis from the U.S. based, prospective PROCEED-CRC clinical trial (NCT06620627) focused on the detection of AAs, which are precancerous polyps with specific features that indicate a higher risk of progression to colorectal cancer. Detecting these lesions early is a critical step in preventing cancer before it develops."
Clinical
2ms
Successful IMvigor011 Trial Achieves 41% Improvement in Overall Survival for Bladder Cancer Patients (Natera Press Release)
"Natera, Inc...today announced results from the randomized, double-blind, phase 3 IMvigor011 clinical trial in muscle-invasive bladder cancer (MIBC). The findings demonstrate that Signatera can expand the adjuvant treatment window and guide the use of adjuvant atezolizumab (Tecentriq®) in MIBC, resulting in improved disease-free survival (DFS) and overall survival (OS). Results will be presented today during a Presidential Symposium at the European Society for Medical Oncology (ESMO) Congress."
New P3 trial
|
Signatera™
2ms
Signatera™ Surveillance Testing Identified 100% of Uterine Cancer Recurrences in Advance of Imaging, New Study Shows (Natera Press Release)
"Natera, Inc...today announced the publication of a new study in the Journal of Clinical Oncology Precision Oncology (JCO PO), validating Signatera for recurrence monitoring and treatment response assessment in patients with early-stage uterine cancer."
Clinical
|
Signatera™
2ms
Natera Announces Publication of Signatera™ Validation Study in Testicular Cancer (Natera Press Release)
''Natera, Inc...today announced the publication of a peer-reviewed manuscript in the Journal of Clinical Oncology – Precision Oncology (JCO PO). The paper features results from a multi-institutional study evaluating circulating tumor DNA (ctDNA) as a prognostic biomarker for patients with germ cell tumors (GCT), including testicular cancer.''
Clinical
|
Signatera™
3ms
Natera Provides Update on Patent Litigation with NeoGenomics (Natera Press Release)
"Natera, Inc...today provided an update regarding its intellectual property litigation with NeoGenomics, Inc...The U.S. District Court for the Middle District of North Carolina issued a ruling invalidating certain claims in two patents that Natera asserted against NeoGenomics’ v1.1 RaDaR test. Natera is evaluating its options, including an appeal and further enforcement with other patents."
Licensing / partnership
|
RaDaR™ assay
4ms
Natera to Present Signatera™ Data at the IASLC World Conference on Lung Cancer (Natera Press Release)
"Natera, Inc...today announced that it will present new data at the 2025 International Association for the Study of Lung Cancer (IASLC) World Conference on Lung Cancer, taking place September 6 – 9 in Barcelona, Spain. The presentations underscore the strong clinical utility of Signatera in lung cancer."
Clinical data
3ms
Signatera™ Test Selected for NRG-Sponsored Phase III ARCHER Trial in Bladder Cancer (Natera Press Release)
"Natera, Inc...today announced the activation of the NRG Oncology trial, ARCHER (NRG-GU015), a randomized, phase III study in muscle-invasive bladder cancer (MIBC). The study is evaluating whether a shorter course of radiation can achieve outcomes comparable to the current standard of care. It prospectively incorporates Signatera, Natera’s personalized, tumor-informed molecular residual disease (MRD) test, as a pre-specified secondary endpoint"
Clinical data
|
Signatera™