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Recruiting

A Study to Test Combination Treatments in People With Advanced Renal Cell Carcinoma - CA018-005

Updated: 15 June, 2020   |   ClinicalTrials.gov

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CONSIDERING THIS TRIAL?
Print this page and the trial guide to help you talk with your doctor.
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 CA018-005
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Trial Details

  • Phase 2

    Phase

  • Gender(s)

  • 18+

    Age Range

  • 30

    Location(s)

  • Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
Experimental: Nivolumab + BMS-813160
Drug: BMS-813160 Biological: Nivolumab
Experimental: Nivolumab + BMS-986205
Biological: Nivolumab Drug: BMS-986205
Active Comparator: Nivolumab + Ipilimumab
Biological: Nivolumab Biological: Ipilimumab
Experimental: Nivolumab + Relatlimab
Biological: Nivolumab Biological: Relatlimab

Key Eligibility Criteria

For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com Inclusion Criteria: - Advanced Renal Cell Carcinoma - Must have at least 1 lesion with measurable disease - Life expectancy of at least 3 months - Karnofsky Performance Status (KPS) must be =>70% Exclusion Criteria: - Patients/subjects with suspected or known central nervous system metastases unless adequately treated - Patients/subjects with autoimmune disease - Patients/subjects who need daily oxygen therapy 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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