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Taking people in United StatesPhase 3

Tests a new drug combination with chemotherapy for extensive-stage small cell lung cancer

Compares a new drug combination with standard treatment in adults with small cell lung cancer.

Plain-language title generated from the registry record
Registry title: 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).

Key facts

Where
Albuquerque, Austin, Bismarck, Cincinnati, Daphne, Durham, Edmonds, Fargo, Fort Myers, Hot Springs, Marietta, Minneapolis, Nashville, Orange City, Peoria, Roanoke, Seattle, Sioux Falls, St. Petersburg, and Tyler, United StatesSee the 20 sites
Phase
Phase 3

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Which best describes your lung cancer?
  • Has the cancer spread to other parts of the body, or is it too advanced to be removed by surgery?
  • Can you look after yourself and are you up and about most of the day?
  • Has your cancer spread to the brain?

Source: NCT06646276, who can take part

Where in United States

  • University of New Mexico Comprehensive Cancer CenterAlbuquerque, United StatesTaking people
  • Texas Oncology - Central/South TexasAustin, United StatesTaking people
  • Sanford Medical CenterBismarck, United StatesTaking people
  • Oncology Hematology CareCincinnati, United StatesTaking people
  • Southern Cancer Center PcDaphne, United StatesTaking people
  • Duke Cancer InstituteDurham, United StatesTaking people
  • Swedish Cancer Institute-EdmondsEdmonds, United StatesTaking people
  • Sanford Fargo Medical CenterFargo, United StatesTaking people
  • Florida Cancer Specialists - SouthFort Myers, United StatesTaking people
  • Hot SpringsHot Springs, United StatesNo longer taking part
  • Northwest Georgia Oncology Centers, a Service of WellStar Cobb HospitalMarietta, United StatesTaking people
  • MinneapolisMinneapolis, United StatesNo longer taking part
  • SCRI Oncology PartnersNashville, United StatesTaking people
  • Mid Florida Hematology and oncology CenterOrange City, United StatesTaking people
  • Illinois Cancer CarePeoria, United StatesTaking people
  • Oncology & Hematology Associates of Southwest Virginia, Inc.Roanoke, United StatesTaking people
  • Swedish Medical CenterSeattle, United StatesTaking people
  • Sanford Cancer CenterSioux Falls, United StatesTaking people
  • Florida Cancer Specialists - NorthSt. Petersburg, United StatesTaking people
  • Texas Oncology - Northeast TexasTyler, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Bristol-Myers Squibb
Trial code
NCT06646276EU 2024-515740-23-00
Record updated
10 November 2026
Original description
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.Read full original descriptionShow less

A Randomized, Double Blind, Multicenter Phase 3 Trial of BMS-986489 (Atigotatug+Nivolumab Fixed Dose Combination) in Combination With Carboplatin Plus Etoposide vs Atezolizumab in Combination With Carboplatin Plus Etoposide as First-Line Therapy in Participants With Extensive-Stage Small Cell Lung Cancer (TIGOS).

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.

Inclusion: 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: 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.

ClinicalTrials.gov NCT06646276 · EU CTIS 2024-515740-23-00