RecruitingPhase 3NCT06646276

A Study to Compare the Efficacy and Safety of BMS-986489 (BMS-986012+ 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).

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.

Checked against the public recordLast updated Aug 14, 2026 · Source: ClinicalTrials.gov

StatusRecruiting
PhasePhase 3
U.S. locations183
SponsorBristol-Myers Squibb
01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Phase 3
Sponsor
Bristol-Myers Squibb
Interventions being studied
Biological: BMS-986489 (BMS-986012+Nivolumab); Biological: Atezolizumab; Drug: Carboplatin; Drug: Etoposide
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

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.

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Southern Cancer Center, PCDaphne, Alabama
  • Local Institution - 0283Hot Springs, Arkansas
  • Florida Cancer Specialists - SouthFort Myers, Florida
  • Mid Florida Hematology and Oncology CenterOrange City, Florida
  • Florida Cancer Specialists - NorthSt. Petersburg, Florida
  • Northwest Georgia Oncology Centers, a Service of Wellstar Cobb HospitalMarietta, Georgia
  • Illinois Cancer CarePeoria, Illinois
  • Local Institution - 0037Minneapolis, Minnesota
  • University of New Mexico Comprehensive Cancer CenterAlbuquerque, New Mexico
  • Duke Cancer InstituteDurham, North Carolina
  • Sanford Medical CenterBismarck, North Dakota
  • Sanford Fargo Medical CenterFargo, North Dakota

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Aug 14, 2026. Always confirm current availability with the study team.

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