Therapeutic ResistAnce and Clonal Evolution Assessed With Liquid Biopsy in ICIs Treated NSCLC Patients

NCT04566432 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 250

Last updated 2024-07-18

No results posted yet for this study

Summary

To evaluate the predictive value of ctDNA in response, relapse for patients treated with immune checkpoint inhibitors or targeted therapy for ALK, ROS1, MET ex14 skipping.

Conditions

  • Lung Neoplasms
  • Lung Cancer, Nonsmall Cell
  • Adenocarcinoma of Lung
  • Squamous Cell Lung Cancer

Interventions

OTHER

Observation

observe the association of ctDNA with efficacy of treatment

Sponsors & Collaborators

  • Shanghai Chest Hospital

    collaborator OTHER
  • Geneplus-Beijing Co. Ltd.

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-07-01
Primary Completion
2024-12-31
Completion
2025-06-30

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 NCT04566432 on ClinicalTrials.gov