This study, known as LUNAR-2, aims to investigate the effectiveness and safety of using TTFields, delivered by the NovoTTF-200T device, concomitantly administered with pembrolizumab and platinum-based chemotherapy for patients with advanced non-small cell lung cancer that has spread to other parts of the body. The primary goals of the study are to assess overall survival and progression-free survival. Secondary objectives include analyzing outcomes based on the specific histology (subtype) of the lung cancer.
A Study of JNJ-86974680 in Participants With Advanced Non-small Cell Lung Cancer
This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.
This trial is no longer recruiting — here are similar active trials
Matched by cancer type/biomarker, currently recruiting.
The purpose of this study is to evaluate the safety and efficacy of Navlimetostat (BMS-986504) monotherapy or in combination with Izalontamab Brengitecan in participants with advanced or metastatic Non-small Cell Lung Cancer (NSCLC) with homozygous MTAP deletion or MTAP loss after progression on prior therapies.
This is a phase Ib/II, multicenter, open-label study of YL201 combined with atezolizumab. The study will include 2 parts. Part 1 of the study is a dose escalation in participants with previously untreated ES-SCLC to determine the safety and tolerability of YL201 in combination with fixed dose of atezolizumab. The planned dose levels of YL201 are 1.2 mg/kg, 1.6 mg/kg and 2.0 mg/kg. Part 2 consists of a dose optimization stage followed by a dose expansion stage. During the dose optimization stage, participants will be randomized 1:1:1 to receive either YL201 at 1.2 mg/kg,1.6 mg/kg or 2.0 mg/kg Q3W in combination with fixed dose of atezolizumab. The decision to initiate the dose expansion stage in Part 2 and choose one or two of the YL201 dose level(s) will be based on the review of safety, PK, and efficacy from the dose optimization stage. Treatment will continue until disease progression, unacceptable toxicity, or withdraw of consent.
The objective of the study is to evaluate the efficacy and safety of BL-M14D1 in combination with Atezolizumab compared to Standard-of-Care Therapy in adult participants with previously untreated extensive-stage small cell lung cancer (ES-SCLC).
About the trial
The purpose of this study is to determine a safe and tolerable dose(s) of JNJ-86974680 for further research in combination with cetrelimab and radiation therapy.
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Pacjenci z potwierdzonym rakiem płuca (niekomórkowym, zaawansowanym, stadium IIIB-IV).
- •Pacjenci z rakiem płuca posiadającym określone mutacje genetyczne, którzy przeszli już wszystkie zalecane terapie celowane i ich choroba postępuje.
- •Pacjenci z rakiem płuca, który nie posiada określonych mutacji genetycznych.
- •Pacjenci, którzy otrzymali już leczenie (immunoterapię anty-PD-1/PD-L1) i chemioterapię opartą na platynie.
- •Pacjenci, którzy wcześniej byli leczeni immunoterapią anty-PD-1/PD-L1 z powodu choroby przerzutowej.
- •Pacjenci, którzy nie byli wcześniej leczeni w ramach tego badania.
- •Pacjenci z prawidłowo działającymi narządami.
✗ Disqualifies
- •Aktywne zmiany w mózgu spowodowane chorobą nowotworową.
- •Czynne choroby autoimmunologiczne.
- •Czynne infekcje.
- •Przebyty przeszczep narządu lub komórek macierzystych.
Simplified criteria — AI translation
Trial details
- Minimum age
- 18 Years
- Last updated (source)
- September 25, 2026
- Sex
- No restrictions
Therapies / drugs in trial
Locations (15)
City of Hope 1
Newnan, United States
Hackensack University Medical Center
Hackensack, United States
Roswell Park Comprehensive Cancer Center
Buffalo, United States
Herbert Irving Comprehensive Cancer Center Columbia University Medical Center
New York, United States
Providence Portland Medical Center
Portland, United States
Thomas Jefferson University
Philadelphia, United States
Next Virginia
Fairfax, United States
Charite Research Organisation GmbH
Berlin, Germany
Universitaetsklinikum Giessen und Marburg GmbH
Giessen, Germany
Severance Hospital Yonsei University Health System
Seoul, South Korea
Samsung Medical Center
Seoul, South Korea
Hosp. Univ. Quiron Dexeus
Barcelona, Spain
Hosp Univ Vall D Hebron
Barcelona, Spain
Hosp. Univ. 12 de Octubre
Madrid, Spain
Hosp. Univ. I Politecni La Fe
Valencia, Spain
Share this trial
Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/7/2026.
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