In this phase III study, the primary objective is to test with a one-sided significance of 5% whether for the treatment of small cell lung cancer (SCLC) patients, brain MRI surveillance alone is non-inferior in terms of overall survival compared to prophylactic cranial irradiation (PCI) combined with brain MRI surveillance in the entire study population.
BMS-986489 (Atigotatug + Nivolumab) vs Durvalumab in Limited-stage Small-cell Lung Cancer (TIGOS-LS)
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 compare the efficacy of zipalertinib versus placebo in participants with early stage resected non-small cell lung cancer (NSCLC) harboring uncommon epidermal growth factor receptor mutation (EGFRmt).
This study is open to adults with extensive-stage small cell lung cancer. The purpose of this study is to find out how well people with this type of cancer tolerate taking study medicines called obrixtamig and pumitamig. Another purpose is to check whether the combination study treatment can make tumours shrink. Obrixtamig and pumitamig are being developed to help the immune system fight cancer. Participants are put into 2 groups. One group gets obrixtamig and pumitamig. The other group gets obrixtamig and pumitamig with standard chemotherapy (carboplatin and etoposide). All study treatments are given as infusions into a vein. This study does not have a fixed duration. Participants can receive obrixtamig and pumitamig for up to 2 years if they benefit from treatment and can tolerate it. Participants visit the study site regularly, with some overnight stays required. During this time, doctors regularly check for health problems that could be caused by the study treatment. They also monitor the size of the tumour(s) and take laboratory tests.
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.
About the trial
This is an open-label, randomized study of BMS-986489 (atigotatug + nivolumab fixed-dose combination) vs durvalumab in limited-stage (LS)-small-cell lung cancer (SCLC) participants. The main goals of this study are to: * Evaluate the efficacy of BMS-986489 vs durvalumab * Evaluate the safety profile of BMS-986489
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Wiek co najmniej 18 lat
- •Potwierdzony histologicznie lub cytologicznie rak płuc typu drobnokomórkowego
- •Ograniczone stadium choroby potwierdzone badaniem PET przed rozpoczęciem chemioterapii
- •Ukończona chemioterapia platynowa z etopoznidem i radioterapia bez progresji choroby
- •Co najmniej 3 cykle chemioterapii
- •Dobrze funkcjonujące organy wewnętrzne i układ krwiotwórczy
- •Chęć stosowania antykoncepcji przez czas badania
✗ Disqualifies
- •Rak drobnokomórkowy spoza płuc
- •Rak duże komórki neuroendokrynne
- •Rak płuc typu drobnokomórkowego z przerzutami
- •Jednoczesne występowanie raka drobnokomórkowego i niedrobnokomórkowego
- •Ciężkie wcześniejsze reakcje alergiczne na podobne leki
- •Uczulenie na składniki leku atigotatug, nivolumab lub durvalumab
- •Zaburzenia neurologiczne obwodowe
Simplified criteria — AI translation
Trial details
- Minimum age
- 18 Years
- Last updated (source)
- September 21, 2026
- Sex
- No restrictions
Therapies / drugs in trial
Locations (34)
Southern Cancer Center
Daphne, United States
Sansum Clinic
Santa Barbara, United States
Florida Cancer Specialists - South
Fort Myers, United States
University of Miami - Sylvester Cancer Center
Miami, United States
Ocala Oncology Center
Ocala, United States
Florida Cancer Specialists - North
Orange City, United States
Cancer Care Centers of Brevard
Palm Bay, United States
Florida Cancer Specialists - East
West Palm Beach, United States
Piedmont Healthcare - Atlanta
Atlanta, United States
Illinois Cancer Specialists
Arlington Heights, United States
Illinois Cancer Care
Peoria, United States
Indiana University Simon Cancer Center
Indianapolis, United States
Baptist Health - Corbin
Corbin, United States
Baptist Health - Lexington
Lexington, United States
Baptist Health - Louisville
Louisville, United States
Minnesota Oncology Hematology
Maple Grove, United States
Missouri Cancer Associates
Columbia, United States
White Plains Hospital Physician Associates
White Plains, United States
Carolina Cancer Research Center
Wilson, United States
Oncology Hematology Care
Cincinnati, United States
The Ohio State University - Arthur James Cancer Hospital & Solove Research Institute
Columbus, United States
Mid Ohio Hem/ Onc dba The Mark H Zangmeister Center
Columbus, United States
Oncology Associates of Oregon (Willamette Valley Cancer Institute and Research Center)
Eugene, United States
Tennessee Cancer Specialists
Knoxville, United States
SCRI Oncology Partners
Nashville, United States
Texas Oncology - West Texas
Amarillo, United States
Texas Oncology- Austin
Austin, United States
Texas Oncology - Gulf Coast
Beaumont, United States
Texas Oncology - DFW
Dallas, United States
Texas Oncology - Northeast Texas
Denison, United States
Texas Oncology - San Antonio
San Antonio, United States
Virginia Cancer Specialists
Fairfax, United States
Virginia Oncology Associates
Norfolk, United States
Blue Ridge Cancer Center (Oncology & Hematology Associates of Southwest VA)
Salem, United States
Share this trial
Data from ClinicalTrials.gov. AI-assisted translation, last sync: 8/18/2026.
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