A Study of Relatlimab Plus Nivolumab Versus Nivolumab Alone in Participants With Advanced Melanoma

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About the study

The purpose of this study is to determine whether relatlimab in combination with nivolumab is more effective than nivolumab by itself in treating unresectable melanoma or melanoma that has spread.
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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. Participants must have histologically confirmed Stage III (unresectable) or Stage IV melanoma, per the AJCC staging system
    2. Participants must not have had prior systemic anticancer therapy for unresectable or metastatic melanoma
    3. Tumor tissue from an unresectable or metastatic site of disease must be provided for biomarker analyses

    EXCLUSION CRITERIA

    Exclusion Criteria:


    1. Participants must not have active brain metastases or leptomeningeal metastases
    2. Participants must not have uveal melanoma
    3. Participants must not have an active, known, or suspected autoimmune 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
    Melanoma
    Age (in years)
    12+
    Phase
    Phase 2/Phase 3
    Participants needed
    714
    Est. Completion Date
    Dec 16, 2025
    Treatment type
    Interventional

    Sponsor
    Bristol-Myers Squibb
    ClinicalTrials.gov identifier
    NCT03470922
    Study number
    CA224047

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