Artera
10 known investors
Artera develops AI-powered diagnostic tests that analyze patient biopsy images to predict therapeutic response in cancer care. The company enables personalized treatment decisions and shared decision-making between clinicians and patients, beginning with localized prostate cancer.
Also known as Artera AI Β· ArteraAI
Founders & leadership
Investors Β· 10
Also in the syndicate Β· 1
Funding
SEC filings, press & company announcements$65M disclosed across 1 round Β· 2025
- $65MraisedDec 2025 Β· 4 sources
Lead Edge Capital (lead), Health Velocity Capital, Heritage Medical Systems, Jackson Square Ventures, Summation Health Ventures
Source β
Source: company announcements and press reports β follow each round's link for the claim.
Company profile
researched Aug 2026Artera is a precision oncology company that develops multimodal artificial intelligence (MMAI) tests combining digitized pathology images with structured clinical data to produce prognostic and predictive outputs for cancer treatment planning. Its lead product, the ArteraAI Prostate Test, is offered in biopsy and post-radical-prostatectomy versions and is intended for adult males 18 or older with localized prostate cancer without clinically or pathologically defined metastases who are candidates for curative-intent management (surgery, radiation therapy with or without systemic therapy, or active surveillance). The test estimates long-term outcomes including distant metastasis, biochemical failure, prostate cancer-specific survival and overall survival, and predicts whether a patient is likely to benefit from short-term androgen deprivation therapy (ST-ADT) alongside radiation. The company also markets an ArteraAI Breast Cancer Test that reports 5- and 10-year distant metastasis risk for early-stage breast cancer and predicts chemotherapy benefit in node-negative patients aged 50 and older.
The prostate test is described as a laboratory-developed test performed at the company's CLIA-certified high-complexity laboratory at 6800 Southpoint Pkwy Suite 950, Jacksonville, Florida. Analysis uses image data from existing H&E slides, requiring no additional staining, procedures or tissue consumption, with results typically available within one to two days of specimen receipt and delivered through an online clinician portal or by fax. Separately, the company states that ArteraAI Prostate received FDA Breakthrough Device Designation and subsequently De Novo marketing authorization as a risk-stratification tool for nonmetastatic prostate cancer regulated as Software as a Medical Device; the company is identified in that context as based in Los Altos, California. In June 2026 Artera announced an expansion of the platform to metastatic hormone-sensitive prostate cancer (mHSPC), described as the first digital pathology-based test providing individual risk estimates to inform mHSPC treatment planning.
Note on name twins: a separate company operating at artera.io β a Santa Barbara-based healthcare patient-communications and agentic AI vendor founded in 2015 by CEO Guillaume de Zwirek β shares the Artera name but is a different business; its funding and metrics are excluded from this profile.
Business model
Artera commercializes AI-based diagnostic tests. The ArteraAI Prostate Test is run as a laboratory-developed test in the company's own CLIA-certified laboratory; clinicians order through an Artera Portal account, and the company's customer success team coordinates shipment of histopathology samples from the pathology lab to the Florida laboratory. Outside the United States, versions of the test are made available through partners.
Test-based revenue reimbursed through payers: Medicare (CMS) has established a payment rate for the ArteraAI Prostate Test, which the company says is fully reimbursed for Medicare patients, and many commercial health plans provide coverage. A financial assistance program is offered to commercially insured patients facing large out-of-pocket costs.
Traction
The prostate test can be ordered in all 50 US states, with partner-enabled availability in Puerto Rico, the United Kingdom, Australia and Israel. Reported clinical validation figures include a cohort in which 34% of patients were identified as likely to benefit substantially from short-term hormone therapy: AI biomarker-positive patients (n=673) showed a hazard ratio of 0.34 (95% CI 0.19-0.63, P<0.001) versus 0.92 (95% CI 0.59-1.43, P=0.71) for biomarker-negative patients (n=1,046), interaction p-value 0.002.
Latest developments
On 2026-06-04 Artera announced expansion of its validated multimodal AI platform to metastatic hormone-sensitive prostate cancer, described as the first digital pathology-based test to provide individual risk estimates for mHSPC treatment planning; the test is listed as now available on the company homepage. The FDA granted De Novo marketing authorization to ArteraAI Prostate for nonmetastatic prostate cancer risk stratification. The company is also listed as exhibiting at the ASTRO 68th Annual Meeting in Boston, September 26-30, 2026.
βΈFull profile β market position, technology, go-to-market, geography, history, risks & controversies
Market position
The company describes ArteraAI Prostate as the first test able to both predict therapy benefit and prognosticate long-term outcomes in localized prostate cancer, the only predictive short-term ADT tool recommended in the NCCN Clinical Practice Guidelines in Oncology for Prostate Cancer, and the first AI test included in those guidelines as a prognostic test. It also cites De Novo FDA authorization as a first-of-its-kind AI-powered digital pathology risk-stratification tool.
Differentiators cited include use of existing H&E slides without additional staining or tissue consumption, one-to-two-day turnaround, validation across multiple large randomized Phase 3 trials, NCCN guideline inclusion, FDA De Novo authorization following Breakthrough Device Designation, Medicare reimbursement, and validation data representing African American patients.
Technology
A multimodal AI (MMAI) platform that ingests digital images of hematoxylin-and-eosin-stained pathology slides together with patient clinical variables to generate prognostic risk estimates and treatment-benefit predictions. Models were trained and validated on large randomized Phase 3 trial datasets with up to 15-year follow-up; published supporting work is cited in NEJM Evidence (Spratt et al., 2023), Nature Digital Medicine (Esteva et al., 2022) and a Journal of Clinical Oncology abstract (Roach et al., 2022). The company reports development data comprising approximately 20% African American men and consistent prognostic performance between African American and non-African American men.
Go-to-market
Direct sales and clinician outreach in the United States, supported by patient-facing education materials, sample test reports, brochures and FAQ resources, plus presence at oncology conferences such as ASTRO. Ordering runs through the Artera Portal after account setup by the sales team. International availability is via partnerships.
Clinicians treating prostate and breast cancer (including radiation oncologists, urologists and pathology labs supplying slides) and their patients. For prostate, the intended population is adult males 18+ with localized, nonmetastatic prostate cancer who are candidates for curative-intent management, plus post-prostatectomy patients with rising PSA; the June 2026 expansion adds metastatic hormone-sensitive prostate cancer. The breast test targets early-stage breast cancer patients, including node-negative patients aged 50 or older.
Geography
United States operations with a CLIA-certified laboratory in Jacksonville, Florida; the company is identified as Los Altos, California in FDA coverage, and a June 2026 announcement was datelined San Francisco. Test ordering is available in all 50 US states, with partner availability in Puerto Rico, the United Kingdom, Australia and Israel.
History
Sources indicate the company's prostate algorithm was developed and validated using data from thousands of patients and tens of thousands of pathology slide images drawn from multiple Phase 3 randomized trials, including NRG Oncology trials and RTOG 9601, with follow-up of up to 15 years. Regulatory milestones described on the company site progress from an FDA Breakthrough Device Designation to De Novo marketing authorization for ArteraAI Prostate. Product scope has expanded from localized prostate cancer to a post-radical-prostatectomy indication, a breast cancer test, and, as announced on 2026-06-04, metastatic hormone-sensitive prostate cancer.
Risks & controversies
Company materials state the ArteraAI Prostate Test as a laboratory-developed test has not been cleared or approved by the FDA, while separately describing De Novo authorization for ArteraAI Prostate as Software as a Medical Device; the relationship between the two is not clarified in the sources. Out-of-pocket cost for commercially insured patients depends on plan terms. Co-founder Felix Feng, MD, is listed on the team page as 'In Memoriam.' A separately operating company also named Artera (artera.io) in healthcare communications creates potential for identity confusion.
Compiled by commissioned research from 8 cited public sources β announcements, filings, and press listed under research sources below.
Key figures
latest reportedCompany-reported or press-reported figures, each dated to when it was claimed β not independently audited.
Timeline Β· 4
launches, deals, and filingsArtera lists the ASTRO 68th Annual Meeting (September 26-30, 2026, Boston) as an upcoming event, with exhibit dates September 27-29, 2026.
Artera announced expansion of its validated multimodal AI platform to mHSPC, described as the first digital pathology-based test providing individual risk estimates to help inform treatment planning in that setting. Announcement datelined San Francisco.
Company states ArteraAI Prostate is the first and only AI test included in the NCCN Clinical Practice Guidelines in Oncology for Prostate Cancer as a prognostic test, and the only predictive short-term ADT tool recommended in those guidelines (referenced versions V.3.2024, V.4.2024 and V.5.2026).
The US FDA granted De Novo marketing authorization to ArteraAI Prostate, an AI-powered risk-stratification tool for patients with nonmetastatic prostate cancer, now regulated as Software as a Medical Device. It followed an earlier FDA Breakthrough Device Designation.
Dated company events from announcements, filings, and press; legal rows summarize public dockets and regulator releases.
In the news
βΈResearch sources Β· 8
primary sources listed
- Arteraartera.ai Β· web
8 public sources were cited for this profile; the first-party ones are listed here.
Frequently asked questions
- What does Artera do?
- Artera builds multimodal AI tests that read digital pathology and clinical data to guide prostate and breast cancer treatment.
- Who founded Artera?
- Artera was founded by Andre Esteva, PhD.
- Who are Artera's investors?
- Artera's investors include Breyer Capital, Coatue Management, Koch Disruptive Technologies, Health Velocity Capital, Jackson Square Ventures, Lead Edge Capital, SUMMATION HEALTH VENTURES, TenOneTen Ventures and 1 more.
- How much funding has Artera raised?
- Artera has disclosed $65M raised across 1 round.



