Price$271.44+6.01 (+2.26%)
01:30 PM07:45 PM
News · 26 weeks152+17%
2026-01-182026-07-12
Mix8190d
- Insider51(63%)
- Other15(19%)
- SEC Filings9(11%)
- Analyst3(4%)
- Earnings2(2%)
- Leadership1(1%)
Latest news
25 items- INSIDERDirector Chapman Rowan E sold $37,101 worth of shares (135 units at $274.82) as part of a pre-agreed trading plan, decreasing direct ownership by 3% to 4,663 units (SEC Form 4)4 - Natera, Inc. (0001604821) (Issuer)
- INSIDERCO-FOUNDER Sheena Jonathan sold $410,825 worth of shares (1,500 units at $273.88) as part of a pre-agreed trading plan (SEC Form 4)4 - Natera, Inc. (0001604821) (Issuer)
- PRFinalized MolDx LCD Includes Expanded Coverage for Natera’s Prospera™ PortfolioSurveillance coverage significantly strengthened with new LCD across kidney, heart, and lung transplantation, expanding coverage for Prospera testing across critical post-transplant settingsNatera, Inc. (NASDAQ:NTRA), a global leader in cell-free DNA and precision medicine, today highlighted the impact of a final local coverage determination (LCD) for molecular testing for solid organ allograft rejection: L40060.The LCD strengthens coverage for Prospera in the surveillance settings. The new policy, which is expected to take effect on August 30, 2026, specifically includes:Kidney: 6 tests in year 1; 4 per year in years 2-3. "For-cause" coverage remains unchanged.Heart: 12 tests in year 1; 4 p
- INSIDERCO-FOUNDER Sheena Jonathan sold $836,898 worth of shares (3,150 units at $265.68) as part of a pre-agreed trading plan, decreasing direct ownership by 1% to 246,202 units (SEC Form 4)4 - Natera, Inc. (0001604821) (Issuer)
- PRNatera Announces IVDR Certification for Signatera™ Across Multiple CancersSignatera is the first personalized molecular residual disease (MRD) test for solid tumors to receive IVDR certification in the EU Natera, Inc. (NASDAQ:NTRA), a global leader in cell-free DNA and precision medicine, today announced that Signatera has received certification as a Class C device under the European Union’s In Vitro Diagnostic Regulation (IVDR). The IVDR represents one of the world’s most rigorous regulatory frameworks for in vitro diagnostic medical devices, replacing the outgoing In Vitro Diagnostic Medical Devices Directive (IVDD). To obtain certification, the Signatera platform — including the assay, specimen collection kit, and associated software — underwent a comprehe
- INSIDEREXECUTIVE CHAIRMAN Rabinowitz Matthew sold $280,000 worth of shares (1,000 units at $280.00) as part of a pre-agreed trading plan (SEC Form 4)4 - Natera, Inc. (0001604821) (Issuer)
- INSIDERSEC. AND CHIEF LEGAL OFFICER Rabinowitz Daniel sold $4,574,431 worth of shares (16,800 units at $272.29) as part of a pre-agreed trading plan, decreasing direct ownership by 9% to 172,294 units (SEC Form 4)4 - Natera, Inc. (0001604821) (Issuer)
- INSIDERPRESIDENT, CLINICALDIAGNOSTICS Moshkevich Solomon sold $818,710 worth of shares (3,000 units at $272.90) as part of a pre-agreed trading plan, decreasing direct ownership by 2% to 134,643 units (SEC Form 4)4 - Natera, Inc. (0001604821) (Issuer)
- SECNatera Inc. filed SEC Form 8-K: Leadership Update8-K - Natera, Inc. (0001604821) (Filer)
- PRSignatera™ MRD Test Predicted Overall Survival Benefit from Chemotherapy in Resected Metastatic Colorectal CancerNewly published study shows Signatera MRD-positive patients lived longer with adjuvant chemotherapy, while MRD-negative patients saw no significant benefit First predictive data for overall survival from GALAXY trial in patients with oligo-metastatic CRC in the liver Natera, Inc. (NASDAQ:NTRA), a global leader in cell-free DNA and precision medicine, today announced the publication of new data in JAMA Oncology, evaluating the utility of Signatera, its personalized molecular residual disease (MRD) test, in patients with resected colorectal liver metastases (CRLM). The data was also presented as an oral presentation at the 2026 European Society for Medical Oncology Gastrointestinal (ESMO
- INSIDERDirector Lynch Thomas J. Jr. was granted 1,905 shares (SEC Form 4)4 - Natera, Inc. (0001604821) (Issuer)
- INSIDERDirector Marcus Gail Boxer was granted 1,669 shares, increasing direct ownership by 27% to 7,852 units (SEC Form 4)4 - Natera, Inc. (0001604821) (Issuer)
- INSIDERDirector Botha Roelof was granted 1,691 shares, increasing direct ownership by 58% to 4,585 units (SEC Form 4)4 - Natera, Inc. (0001604821) (Issuer)
- INSIDERDirector Rosenman Herm was granted 1,677 shares, increasing direct ownership by 39% to 5,927 units (SEC Form 4)4 - Natera, Inc. (0001604821) (Issuer)
- INSIDERDirector Rubin Eric H was granted 75 shares, increasing direct ownership by 4% to 2,204 units (SEC Form 4)4 - Natera, Inc. (0001604821) (Issuer)
- INSIDERDirector Chapman Rowan E was granted 1,674 shares, increasing direct ownership by 54% to 4,798 units (SEC Form 4)4 - Natera, Inc. (0001604821) (Issuer)
- INSIDERDirector Baynes Roy D. was granted 1,646 shares, increasing direct ownership by 9% to 20,158 units (SEC Form 4)4 - Natera, Inc. (0001604821) (Issuer)
- INSIDERDirector Bertagnolli Monica was granted 1,646 shares, increasing direct ownership by 31% to 7,020 units (SEC Form 4)4 - Natera, Inc. (0001604821) (Issuer)
- PRNatera and Aveta Biomics Announce Strategic Partnership Supporting Global Phase 3 Registrational Trial of APG-157 in Head and Neck CancerSignatera™ will be used to evaluate molecular response to APG-157 in the neoadjuvant, induction, and adjuvant settingsNatera, Inc. (NASDAQ:NTRA), a global leader in cell-free DNA and precision medicine, and Aveta Biomics, Inc., a clinical-stage immuno-oncology company advancing first-in-class oral immunotherapies for solid tumors, today announced a strategic partnership supporting AVTA 30-01, Aveta’s global Phase 3 registrational clinical trial evaluating APG-157 in patients with locally advanced head and neck squamous cell carcinoma (LA-HNSCC) (NCT07667296).APG-157 is Aveta's first-in-class oral immunotherapy intended to expand the benefits of immunotherapy to both immune-cold and immune-ho
- INSIDERSEC. AND CHIEF LEGAL OFFICER Rabinowitz Daniel sold $8,455,355 worth of shares (33,600 units at $251.65) as part of a pre-agreed trading plan, decreasing direct ownership by 15% to 189,094 units (SEC Form 4)4 - Natera, Inc. (0001604821) (Issuer)
- INSIDERDirector Rosenman Herm sold $4,132,500 worth of shares (16,530 units at $250.00) as part of a pre-agreed trading plan, decreasing direct ownership by 80% to 4,250 units (SEC Form 4)4 - Natera, Inc. (0001604821) (Issuer)
- ANALYSTBernstein resumed coverage on Natera with a new price targetBernstein resumed coverage of Natera with a rating of Outperform and set a new price target of $310.00
- PRNatera and Eledon Announce Strategic Partnership for Prospera™ Monitoring in Planned Phase 3 Kidney Transplant TrialProspera selected as exclusive donor-derived cell-free DNA (dd-cfDNA) monitoring assay for use in Eledon’s planned Phase 3 trial of tegoprubart in kidney transplantation, expected to initiate in late 2026Natera, Inc. (NASDAQ:NTRA), a global leader in cell-free DNA and precision medicine, and Eledon Pharmaceuticals, Inc. (NASDAQ:ELDN), a clinical stage biotechnology company developing immune-modulating therapies for the management and treatment of life-threatening conditions, today announced a strategic partnership to incorporate Natera’s Prospera kidney transplant assessment test into Eledon’s planned Phase 3 clinical trial of tegoprubart, an investigational therapy designed to prevent organ
- SECSEC Form 144 filed by Natera Inc.144 - Natera, Inc. (0001604821) (Subject)
- PRSignatera™ Receives Regulatory Approval in Japan for Colorectal CancerFirst PMDA-approved molecular residual disease (MRD) test in Japan, supporting the use of Signatera in the adjuvant setting Commercial launch expected by year-end, pending final reimbursement and pricing Natera, Inc. (NASDAQ:NTRA), a global leader in cell-free DNA and precision medicine, today announced that Signatera has received regulatory approval from Japan’s Pharmaceuticals and Medical Devices Agency (PMDA). This approval supports the use of Signatera for patients with colorectal cancer (CRC) in the adjuvant setting and makes Signatera the first PMDA-approved MRD test in Japan. Natera expects to commercially launch Signatera for CRC in Japan by the end of 2026, subject to final p
NTRA FAQ
7 questionsWhat does Natera Inc. do?
Natera, Inc., a diagnostics company, develops and commercializes molecular testing services worldwide. It offers Panorama, a non-invasive prenatal test that screens for chromosomal abnormalities of a fetus with a blood draw from the mother, as well as twin pregnancies for zygosity; Vistara, a single-gene mutations screening test to identify single-gene disorder; Horizon carrier screening to determine carrier status for various genetic diseases; and Spectrum to analyze chromosomal anomalies or inherited genetic conditions during an in vitro fertilization cycle. The company also provides Anora...Where does NTRA stock trade?
Natera Inc. (NTRA) is listed on NASDAQ.What sector and industry is NTRA in?
Natera Inc. operates in the Health Care sector, Medical Specialities industry.When did Natera Inc. go public?
Natera Inc. (NTRA) completed its IPO in 2015.What are analysts saying about NTRA?
Natera Inc. has had 8 recent analyst actions on file. The most recent action was from Bernstein: Outperform on 2026-06-26.What companies are similar to NTRA?
Notable peers in the same industry include UNH (UnitedHealth Group Incorporated), ANTM (Anthem Inc.), ELV (Elevance Health Inc.), CI (The Cigna Group), HUM (Humana Inc.). Compare NTRA side-by-side with any of them on Quantisnow.How can I track NTRA on Quantisnow?
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