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Natera (NTRA)

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Earnings summaries and quarterly performance for Natera.

Research analysts who have asked questions during Natera earnings calls.

Recent press releases and 8-K filings for NTRA.

Natera Submits Signatera CDx PMA to FDA
NTRA
  • Natera has submitted its premarket approval (PMA) to the U.S. Food and Drug Administration (FDA) for Signatera™ CDx.
  • The submission is for the detection of molecular residual disease (MRD) in patients with muscle-invasive bladder cancer (MIBC) who may benefit from treatment with atezolizumab (Tecentriq®).
  • This application is supported by data from the randomized, double-blind, phase 3 IMvigor011 clinical trial, which met its primary endpoint and demonstrated significant improvements in disease-free survival and overall survival for Signatera-positive patients treated with atezolizumab.
  • If approved, Signatera CDx has the potential to be the first companion diagnostic MRD test to guide treatment decisions and improve outcomes for MIBC patients.
2 days ago
Natera Completes Enrollment in Pivotal Heart Transplant Trial
NTRA
New Projects/Investments
Product Launch
  • Natera, Inc. (NTRA) has completed enrollment in its ACES-EMB trial, a randomized-controlled study evaluating the Prospera Heart test for rejection monitoring in heart transplant recipients.
  • This trial is the first randomized-controlled study to compare non-invasive donor-derived cell-free DNA (dd-cfDNA) surveillance with routine invasive biopsies in organ transplantation.
  • Positive results could lead to a fundamental shift in the standard of care, replacing invasive biopsies with the non-invasive Prospera test for approximately 4,500 heart transplants annually in the United States.
7 days ago
Natera Reports Strong Q4 2025 Performance, New Product Launches, and Strategic Investments
NTRA
Revenue Acceleration/Inflection
Product Launch
M&A
  • Natera reported robust Q4 2025 results, with revenues increasing 39% over Q4 2024 to $660 million and Signatera achieving its fastest growth quarter ever with 22,000 clinical MRD tests. The company also generated over $100 million in free cash flow throughout 2025.
  • The company launched new products including the Fetal Focus 21-gene NIPT test and the Latitude tumor-naive MRD product. Natera also acquired Foresight Diagnostics to integrate phased variants technology into Signatera for enhanced sensitivity, with a new version launching in late spring/early summer 2026, expanding into lymphoma and hematologic cancers.
  • Natera is investing an additional $100 million in breast cancer clinical trial evidence development and partnered with Exelixis for the STELLAR Phase 3 trial in colorectal cancer, leveraging its commercial MRD patient base. The company aims to complete enrollment for the FDA-enabling FIND study for early cancer detection in 2026, targeting FDA submission by mid-2027.
  • Natera announced an AI-based foundation model for augmented MRD scoring, expected to roll out mid-2026, and is pursuing expanded Medicare coverage through seven additional Multi-X submissions. The company anticipates 10% year-on-year OPEX growth in 2026, primarily in R&D, as it grows towards profitability.
Jan 14, 2026, 12:30 AM
Natera Reports Strong Q4 2025 Results and Outlines Key 2026 Growth Initiatives
NTRA
Revenue Acceleration/Inflection
Product Launch
New Projects/Investments
  • Natera achieved a record year in 2025 across women's health, organ health, and oncology, with Q4 2025 revenue up 39% over Q4 2024 to $660 million and over $100 million in free cash flow generated throughout 2025.
  • The company reported a record 924,000 units in Q4 2025, driven by strong growth in Signatera MRD, which saw 22,800 growth units over the previous quarter, totaling 22,000 clinical MRD tests in the quarter.
  • Natera plans to roll out an AI-enhanced MRD score mid-year 2026 and launch Signatera genome with phased and structural variants in mid-2026, expanding its oncology offerings.
  • For early cancer detection, Natera aims to complete enrollment for the FDA-enabling FIND study in 2026 with over 35,000 patients, targeting an FDA submission in mid-2027.
  • The company projects 10% year-on-year OPEX growth in 2026, primarily in R&D, and expects continued growth in Signatera Average Selling Prices (ASPs) driven by expanded Medicare reimbursement and biomarker state laws.
Jan 14, 2026, 12:30 AM
Natera reports strong preliminary Q4 2025 financial results and announces new product developments
NTRA
Earnings
Product Launch
M&A
  • Natera reported preliminary total revenues of $660 million for Q4 2025, an increase of 39% over Q4 2024.
  • The company achieved record volumes in Q4 2025 with 924K tests processed and record clinical MRD volumes of 225K tests in the same quarter.
  • Natera launched the 21-gene Fetal Focus single-gene NIPT and Signatera designed on Genome in mid-2025, and acquired Foresight Diagnostics.
  • Key anticipated milestones for 2026 include expanded MolDX coverage, the launch of Signatera in Japan, and collaborations in AI and sequencing.
Jan 14, 2026, 12:30 AM
Natera Reports Strong 2025 Performance and Outlines 2026 Growth Initiatives
NTRA
Revenue Acceleration/Inflection
New Projects/Investments
M&A
  • Natera reported a record year in 2025 across women's health, organ health, and oncology, with Q4 2025 revenue of $660 million, up 39% over the similar period in 2024, and over $100 million in free cash flow generated for the year.
  • The company saw its fastest growth quarter ever for Signatera MRD, with 225,000 clinical MRD tests in Q4 2025, representing 22,800 growth units over the previous quarter.
  • Natera is expanding its oncology offerings by integrating Foresight Diagnostics' phased variants technology into Signatera for a new version launching in late spring/early summer 2026, aiming for ultra-high sensitivity, and moving into the lymphoma and hematologic cancer space.
  • Key 2026 milestones include launching the enhanced Signatera, completing enrollment for the FDA-enabling FIND study in early cancer detection with a target of 35,000+ patients for submission in mid-2027, and expecting continued growth in average selling prices (ASPs) and volume.
  • The company anticipates 10% year-on-year OpEx growth in 2026, primarily in R&D, and expects to grow into profitability, with Signatera ASPs projected to improve in 2026 due to expanded Medicare reimbursement and biomarker laws.
Jan 14, 2026, 12:30 AM
Natera Reports Strong Test Volume and Revenue Growth in Expanding Genomic Testing Market
NTRA
Revenue Acceleration/Inflection
New Projects/Investments
  • The global genomic testing market is projected to reach a valuation of USD 41.34 billion by 2035, growing at a CAGR of 9.54% from USD 16.62 billion in 2025.
  • Natera processed approximately 3.5 million total tests in the full year 2025, marking a 15% increase over 2024, with oncology-specific volumes reaching 800,800 tests in 2025, a 52% year-over-year increase.
  • Financially, Natera's Q4 2024 revenue grew by 53% year-over-year, and the company achieved a 63% gross margin in Q4 2024, reporting cash inflows greater than USD 100 million for the full year 2025.
  • The market is significantly driven by reagents and consumables, which account for over 46.7% of the market share, and sequencing solutions, holding a 66.73% market share.
Jan 13, 2026, 2:30 PM
Natera Announces Breakthrough in MRD-Based Risk Stratification with New AI Model
NTRA
Product Launch
New Projects/Investments
  • Natera announced a breakthrough in MRD-based risk stratification with a new multi-modal AI model designed to enhance its Signatera™ assessment.
  • This AI model integrates longitudinal ctDNA, clinical data, digital pathology, and tumor sequencing data to refine recurrence risk assessment and outcomes prediction.
  • Trained on Natera's proprietary database of approximately 300,000 patients, the approach has demonstrated statistically and clinically significant enhancements.
  • Data from this innovation is expected to be presented at an upcoming conference, with launches anticipated in research and clinical settings.
Jan 13, 2026, 1:00 PM
Natera Announces Preliminary Q4 and Full Year 2025 Financial Results
NTRA
Earnings
Guidance Update
Revenue Acceleration/Inflection
  • Natera, Inc. reported preliminary unaudited total revenues of approximately $660 million for Q4 2025, a 39% increase from Q4 2024, and approximately $2.3 billion for the full year 2025, a 35% increase from FY 2024.
  • The company processed approximately 923,600 tests in Q4 2025, up 17% from Q4 2024, and 3,525,500 tests for the full year 2025, up 15% from FY 2024.
  • Oncology tests, including clinical molecular residual disease (MRD) tests, showed significant growth, with approximately 233,300 oncology tests processed in Q4 2025 (up 55% from Q4 2024) and 800,800 for the full year 2025 (up 52% from FY 2024).
  • Natera achieved cash inflows of approximately $30 million in Q4 2025 and greater than $100 million for the full year 2025.
MetricQ4 2024Q4 2025FY 2024FY 2025
Total Revenues ($USD Millions)$476 $660 $1,700 $2,300
Total Tests Processed (Units)792,800 923,600 3,064,600 3,525,500
Oncology Tests Processed (Units)150,800 233,300 528,200 800,800
Clinical MRD Tests Processed (Units)144,500 225,300 498,300 769,700
Cash Inflows ($USD Millions)$46 $30 N/A>$100
Jan 12, 2026, 9:03 PM
Natera Collaborates with NVIDIA to Scale AI Foundation Models
NTRA
New Projects/Investments
Product Launch
  • Natera announced a new collaboration with NVIDIA to accelerate the development of its multimodal AI foundation model platform for precision medicine.
  • This partnership aims to establish the computational infrastructure required to train and deploy large-scale AI models on complex medical datasets, enabling more precise diagnostics, deeper biological insight, and personalized therapeutic decisions.
  • Natera's AI solutions are anchored by one of the world's largest multimodal, longitudinal oncology datasets, with algorithms like NeoSelect™ and NeoPredict™ demonstrating strong performance in neoantigen and immunotherapy response prediction.
  • The integration of NVIDIA's platforms, including Parabricks, BioNeMo, and NeMo Agent Toolkit, has shown significant efficiency gains, such as an average 75.7% reduction in running time and 59.2% reduction in cost for genomic analysis.
Jan 12, 2026, 3:00 PM