Conquering cancer
with data
Through the power of blood tests, we can uncover clues that allow doctors to discover cancer early and find the best way to treat it.
Through the power of blood tests, we can uncover clues that allow doctors to discover cancer early and find the best way to treat it.
A portfolio of revolutionary liquid precision oncology tests, all with the convenience of a single testing company.3,5
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Guideline-recommended* testing of 74 genes at diagnosis & progression.
5 days†
Guideline-complete** testing of 740+ genes at diagnosis & progression.
7 days†
Residual disease and recurrence monitoring
Stage II or III colorectal, breast, and lung cancer
7 days†
Coming soon to international markets!
Important Note: Guardant Reveal™ and Guardant360® Liquid were developed as a Laboratory Developed Test (LDT), and its performance characteristics determined, by the Guardant Health Clinical Laboratory in Redwood City, CA, USA, which is certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA) as qualified to perform high complexity clinical testing. This test has not been cleared or approved by the US FDA. Guardant Hereditary Cancer was developed as an LDT and is not cleared or approved by the US FDA.
Patient timeline
Early-Stage Cancer
Residual disease detection
and recurrence monitoring
Advanced-Stage Cancer
Treatment selection and monitoring
*Guideline-recommended in oncology, including coverage of all biomarkers specified in the NCCN guidelines for advanced solid tumors.
**Guideline-complete for genomic biomarkers across advanced solid tumors, including emerging biomarkers that may impact treatment planning in the future.
The first and only commercially available liquid biopsy to deliver genomic and epigenomic insights from a single input. †Median turnaround time from sample receipt to results.
References: 1. Guardant Health data on file. October 19, 2023. Guardant Health, Inc. Redwood City, CA. (Reveal MRD positioning.), 2. Parikh AR, Van Seventer EE, Siravegna G, et al. Minimal residual disease detection using a plasma-only circulating tumor DNA assay in patients with colorectal cancer. Clin Cancer Res. 2021;27(20):5586-5594. doi:10.1158/1078-0432.CCR-21-0410, 3. Guardant360® CDx Technical Information. Guardant Health, Inc. Redwood City, CA. February 2023., 4. FDA News Release. FDA approves first liquid biopsy next-generation sequencing companion diagnostic test. August 7, 2020. Accessed October 31, 2022. https://www.fda.gov/news-events/pressannouncements/ fda-approves-first-liquid-biopsy-next-generation-sequencing-companion-diagnostic-test, 5. Guardant360R Assay Specifications. Guardant Health, Inc. Redwood City, CA. October 14, 2024., 6. Guardant Health data on file. September 27, 2024. Guardant Health, Inc. Redwood City, CA.