Concordance of Inivata Liquid Biopsy With Standard of Care Tissue Testing

NCT02906852 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 264

Last updated 2019-05-16

No results posted yet for this study

Summary

The aim of this study is to evaluate the performance of Inivata liquid biopsy analysis compared with standard tissue biopsy analysis for detection of genomic alterations in patients with advanced lung cancer.

Conditions

Sponsors & Collaborators

  • Vector Oncology

    collaborator OTHER
  • Inivata

    lead INDUSTRY

Principal Investigators

  • Ramaswamy Govindan, MD · Washington University School of Medicine

  • Edward Kim, MD · Atrium Health Levine Cancer Institute

  • Clive Morris, MD · Inivata

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-08-01
Primary Completion
2018-05-31
Completion
2018-12-31

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 NCT02906852 on ClinicalTrials.gov