Actively Recruiting

Phase Not Applicable
All Genders
NCT06849518

Study of Longitudinal Plasma PD-L1 Testing With Immunotherapy in Lung Cancer

Led by Ballad Health · Updated on 2025-02-28

30

Participants Needed

1

Research Sites

106 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a prospective pilot study to assess dynamic changes of plasma cell-free RNA (cfRNA) PD-L1 expression in patients with lung cancer undergoing immune checkpoint inhibitor (ICI) based therapy. Results will be correlated with radiographic assessment of immunotherapy treatment response and plasma NGS ctDNA.

CONDITIONS

Official Title

Study of Longitudinal Plasma PD-L1 Testing With Immunotherapy in Lung Cancer

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of stage IV or inoperable stage IIIB non-small cell lung cancer without planned primary radiation therapy
  • Undergoing anti-PD-1 or anti-PD-L1 based immune checkpoint inhibitor treatment
  • Eligible if receiving chemo-immune therapy or dual anti-PD-1/L1 with anti-CTLA-4 regimens including an anti-PD-1/L1 monoclonal antibody
  • Documented informed consent obtained prior to participation
Not Eligible

You will not qualify if you...

  • No treatment with anti-PD-1 or anti-PD-L1 monoclonal antibody
  • Planned primary radiation therapy
  • Small-cell lung cancer histology

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Ballad Health Cancer Care

Kingsport, Tennessee, United States, 37660

Actively Recruiting

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Research Team

C

Charles Mays, PhD, CCRP, CCRC

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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