CA-62 uniquely detects cancer, pre-cancerous conditions (adenomas), and acute inflammatory conditions (ulcers, sarcoidosis) through low differentiated cells production increase - our key distinguisher from competitors
Results from our groundbreaking CA-62 pilot study with 1,005 participants demonstrate exceptional cancer detection capabilities
Study Context: Results based on pilot study of 1,005 participants. Numbers like 100% NPV and sensitivity ranges are study-specific and may vary in larger populations. Important: No medical test achieves perfect accuracy; these results represent current study performance and individual results may vary.
Not Diagnostic: CA-62 is currently a wellness test, not approved for diagnostic use by regulatory agencies.
Comparative Claims: Competitor comparisons marked with * require additional validation studies for regulatory approval.
Comprehensive screening of at-risk population over 45 years with documented occupational cancer exposure.
No patients with no cancers tested positive for CA-62 and none of the CA-62 negative patients were found to have cancer on further clinical testing.
Outperforms all known cancer screening tests especially for asymptomatic early stage cancers with excellent specificity for clinical deployment.
Successfully identified all cancer cases including various types: lymphoma, carcinomas, melanoma, and leukemia.
¹ Sensitivity range based on prospective study of 1,005 asymptomatic participants at 95% specificity threshold
² Negative Predictive Value: No participants with negative CA-62 results were subsequently diagnosed with cancer during clinical follow-up
Study Design: Pilot cancer screening study using CA-62 biomarker - prospective design with comprehensive clinical follow-up
Current research status, ongoing studies, and regulatory pathway for CA-62 technology
Initial pilot study with 1,005 participants has been completed. Results presented at medical conferences for peer review and validation.
Currently positioned as wellness test. Regulatory approval pathway being developed for diagnostic applications with health authorities.
Manuscript preparation in progress for submission to peer-reviewed medical journals. Conference abstracts and posters available for scientific community review.
Research findings being presented at Next Generation Dx Summit 2025 in Washington D.C. for peer review and feedback from diagnostics community.
Complete study population providing context for all reported percentages and statistical measures
Participants with positive CA-62 results, providing denominator for specificity calculations
Actual cancer cases from the 63 CA-62 positive results (27.5% PPV rate)
UCM Technologies is at the forefront of cancer detection innovation, developing the revolutionary CA-62 test - a comprehensive, non-invasive, highly-sensitive early stage cancer screening solution.
Our Universal Cancer Marker (UCM) Technology represents a paradigm shift in cancer screening, offering 90+% sensitivity for stage I&II epithelial cancers (ovarian, pancreatic, colorectal, prostate) while eliminating the need for invasive, costly biopsy procedures.
With our pilot study of 1,005 participants completed across multiple regions, our CA-62 technology demonstrates promising results and is being prepared for larger-scale validation studies to support regulatory approval.
Learn About CA-62 TestingAdvanced biomarker technology for early cancer detection with proven clinical results
Blood Sample Requirement: CA-62 requires a blood sample for testing.
Regulatory Status: CA-62 is a wellness test and is not currently approved for diagnostic use by Health Canada or the FDA.
Study Limitations: 100% sensitivity for cancer in our current study does not preclude the possibility of false negatives in future studies. CA-62 performance may vary in different populations and clinical settings. This test is designed to complement, not replace, standard screening methods.
Avoids invasive, costly, and infection-risky biopsy procedures. Reduces false positives associated with biopsies (1 in 5 biopsies return false positive).
Identifies a small cohort of uninsurable clients with high accuracy, enabling more precise risk assessment. Potentially impacts up to 480,000 cases across North America.
Offers promising accuracy compared to standard tests in pilot study. Currently validated in 1,005-participant study across North America, with larger validation studies planned.
Engages consumers with less-invasive proactive screening, fostering greater receptivity to health management and early intervention.
Advanced biomarker detection using low differentiated cells production increase methodology. Reduces costs and workload in labs while minimizing false positives with our reliable screening tool.
Simple and less-invasive nature makes it suitable for group benefit plans and executive wellness assessments across diverse populations.
Advanced CA-62 biomarker technology delivers superior accuracy with comprehensive risk assessment capabilities for corporate wellness programs.
Comprehensive screening at $300 per test with 88-94% sensitivity¹ and 100% NPV² in current study. May help reduce downstream medical costs through early detection and intervention, though individual results may vary and test performance may differ in larger populations.*
Scale your wellness programs effectively. Simple deployment for group benefit plans and executive assessments.
Screen-and-retest protocol filters transient results. Focus resources on cases that matter most.
CA-62 delivers exceptional clinical performance at $300 per test. Advanced biomarker technology provides comprehensive health insights beyond cancer screening, including pre-cancerous and inflammatory condition detection.
Unlike leading competitors requiring months of setup, UCM integrates into existing wellness programs in weeks. Testing to be performed in CLIA-Certified and CAP-Accredited laboratories. Ready for corporate deployment at $300/test.
Detect cancer early AND identify inflammatory conditions affecting productivity. Potential medical cost benefits at lower cost than leading competitors*.
Test Performance: While CA-62 shows promising results in our pilot study, no medical test achieves perfect accuracy. Results may include false positives and false negatives. Test performance may vary in different populations and clinical settings. Always consult healthcare professionals for interpretation and follow-up care decisions.
Clear ROI metrics showing $649K annual savings per 1,000 employees, direct conference access to leadership team, and transparent cost-benefit reporting for board presentations.
Book an exclusive meeting with UCM Technologies leadership at NGDx Summit 2025
Get in touch with our team for more information about CA-62 technology and partnerships