Earnings summaries and quarterly performance for Natera.
Executive leadership at Natera.
Steven Chapman
Chief Executive Officer and President
Daniel Rabinowitz
Chief Legal Officer and Secretary
John Fesko
President, Chief Business Officer
Matthew Rabinowitz
Executive Chairman
Michael Brophy
Chief Financial Officer
Solomon Moshkevich
President, Clinical Diagnostics
Board of directors at Natera.
Research analysts who have asked questions during Natera earnings calls.
Puneet Souda
Leerink Partners
7 questions for NTRA
Catherine Schulte
Baird
6 questions for NTRA
Daniel Brennan
TD Cowen
5 questions for NTRA
Doug Schenkel
Wolfe Research LLC
4 questions for NTRA
Tycho Peterson
Jefferies
4 questions for NTRA
Casey Woodring
JPMorgan Chase & Co.
3 questions for NTRA
Rachel Vatnsdal Olson
JPMorgan
3 questions for NTRA
Tejas Savant
Morgan Stanley
3 questions for NTRA
Dan Brennan
UBS
2 questions for NTRA
Dan Leonard
UBS Group AG
2 questions for NTRA
David Westenberg
Piper Sandler
2 questions for NTRA
Douglas Schenkel
Wolfe Research, LLC
2 questions for NTRA
Ricki Levitus
Guggenheim Securities, LLC
2 questions for NTRA
Colleen Babington
Wolfe Research, LLC
1 question for NTRA
Daniel Leonard
Stifel Financial Corp.
1 question for NTRA
Daniel Markowitz
Evercore ISI
1 question for NTRA
Matthew Sykes
Goldman Sachs Group Inc.
1 question for NTRA
Matt Sykes
Goldman Sachs Group, Inc.
1 question for NTRA
Noah
Jefferies
1 question for NTRA
Rachel Vatnsdal
JPMorgan Chase & Co.
1 question for NTRA
Subbu Nambi
Guggenheim Securities
1 question for NTRA
Subhalaxmi Nambi
Guggenheim Securities
1 question for NTRA
Recent press releases and 8-K filings for NTRA.
- Natera presented new data on its Signatera MRD test at the American Society of Clinical Oncology Genitourinary Cancers Symposium (ASCO GU), highlighting its potential utility across genitourinary cancers, including for bladder preservation.
- Data from the INDIBLADE and RETAIN trials demonstrated that Signatera-negativity post-therapy was strongly associated with positive outcomes, such as improved bladder-intact event-free survival and metastasis-free survival in muscle-invasive bladder cancer.
- The NIAGARA study included the first-ever presentation of urinary tumor DNA (utDNA) data with clinical correlation, suggesting that the combined assessment of utDNA and circulating tumor DNA (ctDNA) can provide comprehensive risk stratification for residual disease.
- Natera reported Q4 2025 revenue of $666 million, a 40% increase over Q4 2024, and achieved a gross margin of 66.9%. The company generated over $107 million in cash flow for the full year 2025.
- For 2026, Natera initiated guidance expecting revenues between $2.62 billion-$2.7 billion and gross margins between 63%-65%. This revenue guidance implies approximately 25% growth over 2025, excluding true-ups.
- Key product developments include the launch of the Latitude tissue-free MRD test and the 21 gene Fetal Focus single gene NIPT test. The company also integrated phased variant technology from the Foresight Diagnostics acquisition, enhancing Signatera's ultra-sensitivity.
- Natera plans to hold SG&A stable while making targeted investments in R&D and pursuing broader Medicare reimbursement for Signatera to drive future margin expansion.
- Natera reported Q4 2025 revenue of ~$666 million, representing ~40% year-over-year growth compared to Q4 2024, with ~924K total tests processed and ~225K clinical MRD tests.
- The company achieved a gross margin of ~66.9% in Q4 2025, an increase from 62.9% in Q4 2024, and generated ~$107.6 million in cash inflow for the full year 2025.
- For 2026, Natera is establishing a financial outlook with projected revenue between $2.62 billion and $2.70 billion, a gross margin of 63%-65%, and anticipates positive cash inflow.
- Key business highlights in 2025 included the launch of Fetal Focus Single-Gene NIPT and Latitude Tissue-Free MRD, along with Medicare coverage for Signatera in Lung Cancer Surveillance and Signatera Genome.
- Natera reported strong Q4 2025 financial results, with $666 million in revenue, representing approximately 40% revenue growth over Q4 2024, and a gross margin of 66.9%. The company also generated over $107 million in cash flow in 2025.
- The company processed approximately 924,000 tests in Q4 2025, with MRD clinical units growing by 56% compared to Q4 2024, reaching 225,000 tests processed.
- For 2026, Natera initiated guidance projecting revenues between $2.62 billion and $2.7 billion and gross margins between 63% and 65%, expecting another strong cash flow year.
- Significant product developments include the launch of the Latitude tissue-free MRD test and the 21 gene Fetal Focus single gene NIPT test, alongside the integration of phased variant technology into Signatera following the Foresight Diagnostics acquisition.
- Natera reported Q4 2025 revenue of $666 million, representing 40% year-over-year growth, and achieved a record gross margin of 66.9%. The company generated over $107 million in cash flow for 2025.
- For 2026, Natera projects revenues between $2.62 billion and $2.7 billion and gross margins of 63% to 65%. Operating expenses are expected to grow approximately 9.5% at the midpoints.
- Key product advancements include the launch of the 21-gene Fetal Focus single gene NIPT test and the submission of the Latitude tissue-free MRD assay to MolDX. The company also integrated phased variants technology from the Foresight Diagnostics acquisition into its Signatera platform, with a clinical launch planned for this year.
- Natera is actively seeking broader Medicare reimbursement for Signatera, which could provide significant upside beyond the current 2026 guidance.
- Natera reported strong financial results for Q4 2025, with total revenues of $665.5 million, a 39.8% increase year-over-year, and full-year 2025 total revenues of $2,306.1 million, up 35.9% from 2024.
- The company processed approximately 923,600 tests in Q4 2025 and 3,525,500 tests in full-year 2025, reflecting increases of 16.5% and 15.0% respectively, driven by significant growth in oncology tests.
- Natera's gross margin improved to 66.9% in Q4 2025 and 64.7% for the full year 2025, compared to 62.9% and 60.3% in the prior year periods.
- For the full year 2025, the company reported a net loss of $208.2 million, or ($1.52) per diluted share, and achieved positive cash inflow of approximately $107.6 million.
- Looking ahead, Natera anticipates 2026 total revenue between $2.62 billion and $2.70 billion, a gross margin of approximately 63% to 65%, and expects to maintain positive net cash inflow.
- Natera reported total revenues of $2,306.1 million for the full year 2025, an increase of 35.9% compared to the full year 2024, and $665.5 million for the fourth quarter of 2025, up 39.8% from the prior year period.
- The company achieved a gross margin of 64.7% for the full year 2025 and 66.9% for the fourth quarter of 2025, both improvements over the previous year.
- Test volumes saw substantial growth, with 3,525,500 tests processed in full year 2025 (+15.0%) and 923,600 tests processed in Q4 2025 (+16.5%), including a significant increase in oncology tests.
- Natera generated positive cash inflow of approximately $107.6 million for the full year 2025.
- For 2026, Natera anticipates total revenue between $2.62 billion and $2.70 billion and a gross margin of approximately 63% to 65%.
- Natera announced successful results from its Phase 2 SINERGY trial for Signatera™ in recurrent or metastatic head and neck squamous cell carcinoma (R/M HNSCC).
- The trial achieved a strong 63% objective response rate (ORR), which compares favorably to historical controls.
- Signatera-guided treatment reduced chemotherapy exposure for 74% of patients, resulting in a median of 2 chemotherapy cycles, a two-thirds reduction from the current standard of care.
- The study also reported substantially lower severe toxicity (48.1%) compared to historical controls.
- 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.
- 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.
Quarterly earnings call transcripts for Natera.
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