TerminatedNot applicableNCT03477474

Registry of Guardant360® Use and Outcomes In People With Advanced Cancer

The purpose of this registry is to collect data that describes the characteristics of people with advanced cancer for whom the Guardant360 assay is ordered and to observe their clinical outcomes after receiving their results.

Checked against the public recordLast updated Oct 10, 2019 · Source: ClinicalTrials.gov

StatusTerminated
PhaseNot applicable
U.S. locations1
SponsorGuardant Health, Inc.
01
Study overview

What this study is about

Purpose
Not specified
Study type
Observational
Phase
Not applicable
Sponsor
Guardant Health, Inc.
Interventions being studied
Not specified
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

General Inclusion Criteria: 1. 18 Years of age or older 2. Ability to provide written informed consent 3. Blood collected for the most recent Guardant360 test within 8 weeks prior to enrollment General Exclusion Criteria 1. Pregnancy at the time of the qualifying Guardant360 blood collection 2. History of the allogeneic organ or tissue transplant Module 1 (Non-Small Cell Lung Cancer) Inclusion Criteria 1. NSCLC, confirmed by histology or cytology 2. Advanced disease, defined as: stage IIIB or IV NSCLC at the time of the qualifying Guardant360 blood collection; or for subjects with an initial diagnosis of Stage I-IIIA disease, NSCLC that is recurrent or metastatic at the time of the qualifying Guardant360 blood collection 3. One of the following conditions at the time of the qualifying Guardant360 blood collection: * No prior systemic therapy for advanced disease OR * All three of the following conditions: 1\. A history of prior systemic therapy for advanced disease, 2. Disease progression within the previous four weeks, \& 3. No new systemic therapy for advanced disease Exclusion Criteria Subjects with a diagnosis or history of any cancer involving the lung that is not classified as NSCLC, including but not limited to small cell carcinoma, neuroendocrine or carcinoid tumor, lymphoma, mesothelioma, metastatic non-lung carcinoma, or cancer of unknown primary.

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Holy CrossFort Lauderdale, Florida

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Oct 10, 2019. Always confirm current availability with the study team.

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