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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: 30 January, 2019   |   ClinicalTrials.gov

Print Friendly Summary

CONSIDERING THIS TRIAL?
Print this page and the trial guide to help you talk with your doctor.
Use the Study Participants 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 CA028-001
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Trial Details

  • Phase 1

    Phase

  • Gender(s)

  • 18+

    Age Range

  • 2

    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