SIBYL: obServation of Therapy Response With lIquid BiopsY evaLuation

Status Recruiting

Clinical Trial Summary

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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05935384
Study type	Observational
Source	Guardant Health, Inc.
Contact	Clinical Trial Operations
Phone	8556988887
Email	sibyl@guardanthealth.com
Status	Recruiting
Phase
Start date	October 25, 2023
Completion date	August 30, 2029

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