Image

LUNAR-4: Effect of Tumor Treating Fields (TTFields) (150 kHz) Concurrent With Pembrolizumab for Treatment of Metastatic Non-small Cell Lung Cancer (NSCLC)

LUNAR-4: Effect of Tumor Treating Fields (TTFields) (150 kHz) Concurrent With Pembrolizumab for Treatment of Metastatic Non-small Cell Lung Cancer (NSCLC)

Not Recruiting
18 years and older
All
Phase 2

Powered by AI

Overview

The purpose of the study is to test the effectiveness and safety of TTFields therapy, delivered using the NovoTTF-200T device, concomitant with pembrolizumab in subjects with metastatic NSCLC previously treated with a PD-1/PD-L1 inhibitor and platinum-based chemotherapy.

Eligibility

INCLUSION CRITERIA:

  • ≥18 years of age
  • Histologically or cytologically confirmed diagnosis of NSCLC.
  • Documented positive tumor PD-L1 expression (TPS≥1%).
  • Eastern Cooperative Oncology Group (ECOG) Score of 0-1.
  • Diagnosis of radiological progression while on or after first platinum-based systemic therapy administered for advanced or metastatic disease.
  • Subjects must have received one line of PD-1/PD-L1 inhibitor therapy for advanced or metastatic NSCLC. PD-1/PD-L1 inhibitor may have been given alone or in combination with other therapy.
  • Subjects who received PD-1/PD-L1 inhibitor for advanced disease, must have had a best response on PD-1/PD-L1 inhibitor of stable disease (SD), partial response (PR) or complete response (CR).
  • Subjects must have experienced disease progression more than 84 days following Cycle 1 Day 1 (C1D1) of their most recent PD-1/PD-L1 inhibitor therapy.

EXCLUSION CRITERIA - All individuals meeting any of the following exclusion criteria will be excluded from study participation:

  • Mixed small cell and NSCLC histology.
  • Subject must not have leptomeningeal disease or spinal cord compression.
  • Subject must not have untreated, symptomatic brain metastases, or residual neurological dysfunction.
  • Subjects must not have received more than one line of PD-1/PD-L1 inhibitor for advanced disease.
  • Subjects with a known sensitizing mutation for which the Food and Drug Administration (FDA)-approved targeted therapy for NSCLC exists (e.g., EGFR, ALK, ROS1) are excluded unless previously received at least one of the approved therapy(ies).
  • Subjects with more than 2 lines of therapy in the advanced setting.
  • Pregnant or breastfeeding.
  • Implantable electronic medical devices (e.g. pacemaker, defibrillator) in the upper torso.
  • Known allergies to medical adhesives or hydrogel.

Study details
    Non-Small Cell Lung Cancer (NSCLC)

NCT06558799

NovoCure GmbH

21 November 2025

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.