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Clinical Trials in the UK / NCT06646276
Recruiting Phase 3

A Study to Compare the Efficacy and Safety of BMS-986489 (Atigotatug+ Nivolumab Fixed Dose Combination) in Combination With Carboplatin Plus Etoposide to That of Atezolizumab With Carboplatin Plus Etoposide as First-Line Therapy in Participants With Extensive-Stage Small Cell Lung Cancer (TIGOS).

NCT06646276 · tracked via the Priya Life Science UK tracker
Sponsor
Bristol-Myers Squibb
Phase
Phase 3
Started
2025-02-25
Last updated
2026-09-11

Condition(s) studied

Extensive-Stage Small Cell Lung Cancer

Investigational drug(s) / intervention(s)

BMS-986489 (Atigotatug+Nivolumab)AtezolizumabCarboplatinEtoposide

BMS-986489 (Atigotatug+Nivolumab): Specified dose on specified days

Atezolizumab: Specified dose on specified days

Carboplatin: Specified dose on specified days

Etoposide: Specified dose on specified days

Study summary

The Purpose of the Study is to Compare the Efficacy and Safety of BMS-986489 (Anti-fucosyl-GM1+ Nivolumab Fixed Dose Combination) in Combination with Carboplatin plus Etoposide to that of Atezolizumab with Carboplatin plus Etoposide as First-Line Therapy in Participants with Extensive-Stage Small Cell Lung Cancer.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria * Participants must have diagnosis of Extensive-Stage Small Cell Lung Cancer (ES-SCLC). * Participants must be Healthy enough to do their normal activities with little or no help based on the ECOG performance scale. * Participants must have at least one tumor that can be measured using special imaging techniques like a CT scan or MRI at a site other than the brain and nervous system Exclusion Criteria * Participants have already received certain types of treatment for extensive stage small cell lung cancer * Participants have certain health conditions, like spread of small cell lung cancer to the brain that are causing symptoms, certain lung diseases, heart diseases, infections, autoimmune diseases, other cancers, or a type of nerve damage called peripheral sensory neuropathy * Other protocol-defined Inclusion/Exclusion criteria apply.

Primary outcome measure(s)

Trial sites (183)

FacilityCityRegionStatus
Southern Cancer Center, PC Daphne Alabama Recruiting
Local Institution - 0283 Hot Springs Arkansas Completed
Florida Cancer Specialists - South Fort Myers Florida Recruiting
Mid Florida Hematology and Oncology Center Orange City Florida Recruiting
Florida Cancer Specialists - North St. Petersburg Florida Recruiting
Northwest Georgia Oncology Centers, a Service of Wellstar Cobb Hospital Marietta Georgia Recruiting
Illinois Cancer Care Peoria Illinois Recruiting
Local Institution - 0037 Minneapolis Minnesota Withdrawn
University of New Mexico Comprehensive Cancer Center Albuquerque New Mexico Recruiting
Duke Cancer Institute Durham North Carolina Recruiting
Sanford Medical Center Bismarck North Dakota Recruiting
Sanford Fargo Medical Center Fargo North Dakota Recruiting
Oncology Hematology Care Cincinnati Ohio Recruiting
Sanford Cancer Center Sioux Falls South Dakota Recruiting
SCRI Oncology Partners Nashville Tennessee Recruiting
Texas Oncology - Central/South Texas Austin Texas Recruiting
Texas Oncology - Northeast Texas Tyler Texas Recruiting
Oncology & Hematology Associates of Southwest Virginia, Inc. Roanoke Virginia Recruiting
Swedish Cancer Institute - Edmonds Edmonds Washington Recruiting
Swedish Medical Center Seattle Washington Recruiting
Local Institution - 0079 Ciudad Autónoma de Buenos Aires Buenos Aires Completed
Local Institution - 0077 ABB Buenos Aires F.D. Completed
Local Institution - 0100 Buenos Aires Buenos Aires F.D. Withdrawn
Local Institution - 0080 CABA Buenos Aires F.D. Active Not Recruiting
Local Institution - 0094 Río Cuarto Córdoba Province Active Not Recruiting
Local Institution - 0202 Campbelltown New South Wales Active Not Recruiting
Local Institution - 0106 Penrith New South Wales Active Not Recruiting
Local Institution - 0105 Brisbane Queensland Active Not Recruiting
Local Institution - 0190 Ballarat Central Victoria Completed
Local Institution - 0175 Murdoch Western Australia Active Not Recruiting
Local Institution - 0253 Graz Styria Active Not Recruiting
Local Institution - 0251 Wels Upper Austria Completed
Local Institution - 0252 Linz Austria Active Not Recruiting
Local Institution - 0255 Rankweil Austria Active Not Recruiting
Local Institution - 0198 Brussels Bruxelles-Capitale, Région de Active Not Recruiting
Local Institution - 0091 Ghent Oost-Vlaanderen Active Not Recruiting
Local Institution - 0187 Sint-Niklaas Oost-Vlaanderen Active Not Recruiting
Local Institution - 0092 Liège Belgium Active Not Recruiting
Local Institution - 0166 Fortaleza Ceará Active Not Recruiting
Local Institution - 0165 Porto Alegre Rio Grande do Sul Active Not Recruiting

+ 143 more sites — see the full list on the official registry below.

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06646276 on ClinicalTrials.gov ↗ ← All trials in the UK