Guardant360® Related Clinical Outcomes in Patients Who Share Medical Records-Breast Cancer

NCT04436393 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 109

Last updated 2022-06-22

No results posted yet for this study

Summary

The purpose of this study is to observe the routine clinical care of patients who have been diagnosed with breast cancer and have undergone Guardant360 testing.

Conditions

Interventions

DIAGNOSTIC_TEST

Guardant360 test

tumor cfDNA testing

Sponsors & Collaborators

  • Guardant Health, Inc.

    lead INDUSTRY

Principal Investigators

  • Victoria M Raymond, M.S. · Guardant Health, Inc.

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-07-02
Primary Completion
2022-03-17
Completion
2022-03-17

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04436393 on ClinicalTrials.gov