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NCT06849518 · ClinicalTrials.gov registry record · NA

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

A NA study of Lung Cancer (NSCLC), sponsored by Ballad Health.

Recruiting
Registry status
NA
Development phase
30
Enrollment target
1
Study location

NCT06849518 is a NA study of Lung Cancer (NSCLC) that is actively recruiting participants, run by Ballad Health. The registered enrollment target is 30 participants, below the 211-participant average among 7 other Lung Cancer (NSCLC) trials with a reported enrollment target (86% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06849518, a NA study of Lung Cancer (NSCLC), is actively recruiting participants, sponsored by Ballad Health.

RECRUITING
Registry status
NA
Development phase
30 participants
Enrollment target
1
Study location

Study Summary

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 Studied

Interventions

  • DIAGNOSTIC_TEST Circulogene liquid biopsy testing

Study Locations (1)

Tennessee

  • Ballad Health Cancer Care - Kingsport

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2025-02-11
Est. Completion 2027-03-01
Phase NA

Sponsor

Ballad Health

2 total trials

What the Registry Record Tells You About NCT06849518

The ClinicalTrials.gov registry entry for NCT06849518 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 211-participant average among 7 other Lung Cancer (NSCLC) trials with a reported enrollment target (86% lower). The listed sponsor is Ballad Health, which has 2 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Lung Cancer (NSCLC) appearing as the primary indexed condition, and to 1 intervention - of which Circulogene liquid biopsy testing is the first listed.

NCT06849518 reports 1 study location spanning 1 distinct geographic area - top geographies include Tennessee.

Frequently Asked Questions

What is clinical trial NCT06849518 about?

NCT06849518 is a clinical study titled "Study of Longitudinal Plasma PD-L1 Testing With Immunotherapy in Lung Cancer". 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...

What is the current status of trial NCT06849518?

This trial is currently recruiting. It is a NA study. The enrollment target is 30 participants. The study started on 2025-02-11. Estimated completion is 2027-03-01.

What conditions does trial NCT06849518 study?

This clinical trial studies the following conditions: Lung Cancer (NSCLC).

What interventions are being tested in trial NCT06849518?

The interventions under investigation include: Circulogene liquid biopsy testing (DIAGNOSTIC_TEST).

Who is sponsoring clinical trial NCT06849518?

This trial is sponsored by Ballad Health, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06849518 being conducted?

This trial has 1 study location across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.