Guardant360

1 clinical trials involving this therapy/drug

This is not medical advice - consult your oncologist

Descriptions are automatically translated with AI assistance. Always verify details in the original on ClinicalTrials.gov and consult your treating physician.

RecruitingUnknown phaseBreast cancerLung cancerColorectal cancerTriple negative (TNBC)HER2 positiveHormone receptor positive (HR+)Metastatic / advanced

SIBYL: obServation of Therapy Response With lIquid BiopsY evaLuation

NCT05935384ClinicalTrials.gov ↗

The purpose of SIBYL is to generate clinical validity data for the ability of a future version of Guardant360 developed by Guardant Health to measure response to systemic therapy in patients with unresectable advanced solid tumors. It is necessary to collect clinical data points and treatment outcomes in order to demonstrate clinical validity for longitudinal monitoring with ctDNA and correlation of ctDNA dynamics with therapeutic response, as evaluated by standard methods, including RECIST 1.1 and CT scan measurements.

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