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Active, Not Recruiting

A Safety Study of Lirilumab in Combination With Nivolumab or in Combination With Nivolumab and Ipilimumab in Advanced and/or Metastatic Solid Tumors - CA223-030

Updated: 14 May, 2020   |   ClinicalTrials.gov

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CONSIDERING THIS TRIAL?
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Use the Study Participant's 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 CA223-030
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Trial Details

  • Phase 1

    Phase

  • Gender(s)

  • 20+

    Age Range

  • Active, Not Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
Experimental: Part 2 Combination Therapy
Biological: Lirilumab Biological: Ipilimumab Biological: Nivolumab
Experimental: Part One Combination Therapy
Biological: Nivolumab Biological: Lirilumab

Key Eligibility Criteria

Inclusion Criteria: For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com - Participants must have histologic or cytologic confirmation of a solid malignancy that is advanced (metastatic and/or unresectable) - Presence of at least 1 lesion with measurable disease as defined by response evaluation criteria in solid tumors version 1.1 (RECIST v1.1) criteria for response assessment - The Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 Exclusion Criteria: - Participants with untreated central nervous system (CNS) metastases - Participants with an active, known, or suspected autoimmune disease - Uncontrolled or significant cardiovascular disease Other protocol defined inclusion/exclusion criteria could apply

We strongly recommend you contact BMS to report Side Effects (Adverse Events)
Side Effects (Adverse Events) and other reportable events are defined here
Report Side Effects (Adverse Events) or Product Quality Complaints: Medical Information

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