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

Last updated: April 1, 2025
Sponsor: NovoCure GmbH
Overall Status: Active - Recruiting

Phase

2

Condition

N/A

Treatment

Pembrolizumab

NovoTTF-200T

Clinical Study ID

NCT06558799
EF-50
  • Ages > 18
  • All Genders

Study Summary

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 Criteria

Inclusion

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 Design

Total Participants: 69
Treatment Group(s): 2
Primary Treatment: Pembrolizumab
Phase: 2
Study Start date:
October 14, 2024
Estimated Completion Date:
December 31, 2026

Connect with a study center

  • Universitätsklinik f. Innere Medizin III

    Salzburg,
    Austria

    Active - Recruiting

  • Universitätsklinik f. Innere Medizin III, Salzburg

    Salzburg,
    Austria

    Active - Recruiting

  • Vitkovicka Nemocnice

    Ostrava, 1192
    Czechia

    Active - Recruiting

  • FN Motol

    Praha, 150 06
    Czechia

    Active - Recruiting

  • Montpellier University Hospital

    Montpellier, 34295
    France

    Active - Recruiting

  • Humanitas Gavazzeni Bergamo-U.O.Farmacia-Edificio D Piano -1

    Bergamo,
    Italy

    Active - Recruiting

  • AOUS Policlinico Le Scotte U.O.C. Immunoterapia Oncologica

    Siena, 53100
    Italy

    Active - Recruiting

  • Rijnstate Ziekenhuis

    Arnhem,
    Netherlands

    Active - Recruiting

  • Pratia MCM Kraków

    Kraków,
    Poland

    Active - Recruiting

  • MS Pneumed Janusz Milanowski, Katarzyna Szmygin-Milanowska Spó?ka Jawna

    Lublin,
    Poland

    Active - Recruiting

  • Hospital Universitario Arnau de Vilanova

    Lleida,
    Spain

    Active - Recruiting

  • Clínica Universidad de Navarra, Madrid

    Madrid, 28027
    Spain

    Active - Recruiting

  • Hospital Regional Universitario de Malaga (Hospital Civil)

    Málaga,
    Spain

    Active - Recruiting

  • Clínica Universidad de Navarra

    Pamplona, 31008
    Spain

    Active - Recruiting

  • Hospital Universitario Virgen del Rocio

    Sevilla,
    Spain

    Active - Recruiting

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