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Recruiting

An Adaptive Study to Match Patients With Solid Tumors to Various Immunotherapy Combinations Based Upon a Broad Biomarker Assessment - CA028-001

Updated: 16 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.
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Trial Details

  • Phase 1

    Phase

  • Gender(s)

  • 18+

    Age Range

  • 1

    Location(s)

  • Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
Experimental: Arm A
Biological: Lirilumab Biological: Nivolumab
Experimental: Arm B
Biological: Relatlimab Biological: Nivolumab
Experimental: Arm C
Biological: Cabiralizumab Biological: Nivolumab
Experimental: Arm D
Biological: Ipilimumab Biological: Nivolumab
Experimental: Arm E
Biological: anti-GITR Biological: Nivolumab
Experimental: Arm F
Drug: IDO1 Inhibitor Biological: Nivolumab
Experimental: Arm G
Radiation: Radiation Therapy Biological: Nivolumab

Key Eligibility Criteria

For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com Inclusion Criteria: - Participants must have an ECOG performance status of less than or equal to 1 - Participants must have had prior therapy - Participants must have at least 2 lesions with measurable disease as defined by RECIST Version 1.1 Exclusion Criteria: - Participants must not have suspected, known, or progressive CNS metastases, have untreated CNS metastases, or have the CNS as the only site of disease - Participants must not have carcinomatous meningitis - Participants must not have other active malignancy requiring concurrent intervention 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