For Healthcare Professionals

An Investigational Study of Immunotherapy Combinations With Chemotherapy in Patients With Gastric or Gastroesophageal Junction (GEJ) Cancers

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About the study

The purpose of this study is to determine the efficacy and safety of investigational drug relatlimab plus nivolumab in combination with chemotherapy in participants with unresectable, untreated, locally advanced or metastatic gastric or GEJ cancer.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

  • For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com
  • Inclusion Criteria:


    1. Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1
    2. Histologically- or cytologically-confirmed diagnosis of unresectable and either locally advanced, or metastatic gastric cancer or GEJ adenocarcinoma
    3. No prior treatment with systemic treatment (including HER 2 inhibitors) given as primary therapy for unresectable and either locally advanced, or metastatic GC or GEJ adenocarcinoma
    4. Tumor tissue must be provided for biomarker analyses

    EXCLUSION CRITERIA

    Exclusion Criteria:


    1. Participants with HER2 positive status
    2. Participants with known untreated central nervous system (CNS) metastases
    3. Uncontrolled or significant cardiovascular disease

    Other protocol defined inclusion/exclusion criteria could apply


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    Study Locations

    Enter your ZIP code/Postal code/PIN code to locate study sites near you:

    How to Apply


    Contact the study center to learn if this study is a good match for you.

    Study’s details


    Contition

    Gastric Cancer,Cancer of the Stomach,Esophagogastric Junction

    Age (in years)

    18+

    Phase

    Phase 2

    Participants needed

    274

    Est. Completion Date

    Dec 1, 2024

    Treatment type

    Interventional


    Sponsor

    Bristol-Myers Squibb

    ClinicalTrials.gov identifier

    NCT03662659

    Study number

    CA224060

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