Access Programs

Through Project ACTT, Canexia Health is speeding up cancer testing for targeted treatment selection during and beyond COVID-19 through a minimally invasive circulating tumor (ctDNA) DNA assay. The assay, which requires a blood sample, is available as an alternative to some surgical tissue biopsies for patients with advanced lung, breast, or colorectal cancer

Learn more about Project ACTT

Where Oncology Meets AI

We pair the latest advances in oncology with machine learning to provide cancer researchers and professionals with the insights needed to make informed decisions

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Our Partners

“We have found the FIND-IT assay to be a reliable, quick and cost-effective tool for identifying driver mutations in fixed tissue samples from across Australia. This has had direct implications for identifying patients suitable for targeted therapies, especially those with lung cancer, colorectal cancer and melanoma. However, the scope of the test is such that there is also interest in the panel for patients with a variety of other cancers, including breast and endometrial cancers.” Professor Graeme Suthers, Sonic Genetics

Our Solutions

Follow It®

A minimally invasive option for biopsy, Follow It can also be used to monitor cancer progression or investigate treatment resistance.

Learn About Follow It


Rapid, cost-effective, and clinically actionable, Fusions allows you the flexibility to isolate and interrogate relevant fusions.

Learn About Fusions

Canexia Health Insights Platform

Make more informed treatment decisions by using detailed results for therapeutic recommendations and expertly curated clinical trials information provided in our comprehensive reporting software.

Learn About Our Reports

Your Labs, Our Technology

Perform sophisticated NGS oncology profiling right from your laboratory without the large upfront investment. Pairing our cloud-based analytics, interpretation, and reporting platform allows partner labs access to our proprietary informatics software suite. This suite covers the full stack of molecular and computational quality assurance, genome analytics, mutation interpretation, and report generation.

Discover Our Technology

Recent Resources

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Contact us today to learn about our end-to-end solution, from mutation identification to auto-generated clinical reports.

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