ivSYTE Diagnostics is building the world's broadest-spectrum blood-based multi-cancer early detection platform — powered by VitaSpectra AI and 200+ biomarker signatures.
Over 75% of cancers are detected at late stages when survival rates drop below 25%. Early detection is the single most impactful intervention in oncology.
52% of lung cancers are detected at distant stage with only 9.7% 5-year survival. Current screening tools miss early signals entirely.
A single blood draw analyzes 200+ biomarker signatures across RBC, immune, protein, cfDNA, and metabolomics panels — detecting cancer 3.2 years earlier.
At $490 — nearly half the price of competitors — ivSYTE makes multi-cancer screening accessible to hospitals, clinics, and high-risk individuals alike.
LSTM + Gradient Boosting models track 180+ markers over time, creating a personalised baseline and risk score delivered through a physician dashboard.
A six-step AI workflow from blood draw to physician dashboard, integrating the broadest spectrum of biomarker classes in any MCED test.
RDW · MCV · Hgb · CAIX · Eryptosis · Band3 — 40+ cancer types, 14–36 month lead time.
NLR · PLR · SII · NK cells · Tregs · MDSCs · CD4/CD8 — 60+ cancer types, 12–38 months.
CEA · CA-125 · VEGF · AFP · PSMA · KRAS · TP53 · ctDNA — 200+ types, 6–36 months.
2-HG · Sarcosine · Kynurenine · Lactate · TEP mRNA · cfRNA-TERT — 50+ types, 10–36 months.
NLR + cfDNA + Metabolomics ensemble — 200+ cancer types with 24–42 month lead time.
Personalised longitudinal risk scores, flagging high-risk alerts with 97.2% confirmation rate.
A multidisciplinary team combining oncology, computational biology, AI, and business expertise.
We are currently raising a $125M Series B with a $40M anchor ask. Our full CFO investor dashboard covers market opportunity, revenue forecast, competitive landscape, use of proceeds, and financial projections.
View CFO Investor Dashboard →From founded startup to market leader in multi-cancer early detection — a decade of disciplined execution.
ivSYTE incorporated. Seed funding secured from angel investors to begin platform R&D.
VitaSpectra AI core model validated with 91% sensitivity across internal datasets.
First institutional funding round secured to accelerate biomarker engine development and expand the clinical team.
Investigational Device Exemption granted by FDA for clinical trial initiation.
Series A2 extension secured to fund expanded clinical trials, MGB partnership negotiations, and compute infrastructure.
Mass General Brigham pilot studies completed. Pre-Market Approval obtained Q4 2025.
Venture debt secured to fund launch preparation: computational scale-up and headcount growth.
National rollout through hospital and clinic networks. Life cycle management begins with biomarker panel expansion.
Reach break-even 2029, profitability 2030. Expand to EU and APAC markets. Target $250M revenue by 2033.