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Recruiting

An Investigational Immuno-therapy Study to Test Combination Treatments in Patients With Advanced Non-Small Cell Lung Cancer - CA018-001

Updated: 10 May, 2018   |   ClinicalTrials.gov

CONSIDERING THIS TRIAL?
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Use the trial guide to navigate the process of participating in a clinical trial. Understand key factors to consider before deciding and get questions to ask your healthcare team.
Print this page CA018-001
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Trial Details

  • Phase 2

    Phase

  • Gender(s)

  • 18+

    Age Range

  • 43

    Location(s)

  • Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
Active Comparator: Nivolumab
Biological: Nivolumab
Experimental: Nivolumab & BMS-986205
Drug: BMS-986205 Biological: Nivolumab
Experimental: Nivolumab & Dasatinib
Drug: Dasatinib Biological: Nivolumab
Experimental: Nivolumab & Ipilimumab
Biological: Ipilimumab Biological: Nivolumab
Experimental: Nivolumab & Relatlimab
Biological: Relatlimab Biological: Nivolumab

Key Eligibility Criteria

For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com Inclusion Criteria: - Advanced Non Small Cell Lung Cancer (NSCLC) - Eastern Cooperative Oncology Group (ECOG) Performance status of ≤ 1 - Life expectancy of at least 3 months from most recent chemotherapy or immunotherapy treatment - Must have at least 1 lesion with measurable disease Exclusion Criteria: - Subjects with certain mutations that have not been treated with a targeted therapy prior to enrollment - Subjects who need daily oxygen therapy - People with autoimmune disease Other protocol defined inclusion/exclusion criteria could apply

Have questions? Call 855-907-3286 or Email Us

Have questions?
Call 855-907-3286 or Email Us