T790M Mutation on ctDNA in Patients With NSCLC After EGFR-TKI Failure

NCT02418234 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 314

Last updated 2018-03-12

Study results available
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Summary

The purpose of this study is to compare the frequency and abundance of T790M mutation among the different Clinical modes of EGFR-TKI failure.

Conditions

  • Non-small Cell Lung Cancer Stage III
  • Non-Small-Cell Lung Cancer Metastatic

Interventions

OTHER

mutation detection

OTHER

ARMS and ddPCR

GENETIC

ctDNA analysis

Sponsors & Collaborators

  • First People's Hospital of Hangzhou

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-03-31
Primary Completion
2016-04-30
Completion
2017-11-30

Countries

  • China

Study Locations

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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 NCT02418234 on ClinicalTrials.gov