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Recruiting

A Phase 1, Bioavailability Study of Relatlimab in Combination With Nivolumab - CA224-087

Updated: 3 August, 2020   |   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 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.

Trial Details

  • Phase 1

    Phase

  • Gender(s)

  • 18+

    Age Range

  • Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
Experimental: nivolumab + relatlimab + rHuPH20
Drug: relatlimab Drug: rHuPH20 Drug: nivolumab

Key Eligibility Criteria

For more information regarding Bristol Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com Inclusion Criteria: - Histologic or cytologic confirmation of (unresectable and/or metastatic) advanced solid tumors - Melanoma - Metastatic squamous or non- squamous non-small cell lung cancer (NSCLC) - Gastric adenocarcinoma (includes gastro-esophageal junction) - Hepatocellular carcinoma (HCC) - Squamous cell carcinoma of the head and neck (SCCHN) - Renal cell carcinoma (RCC) - Bladder cancer - Participants must have received available standard therapies - Women and men must agree to follow instructions for method of contraception - Measureable disease as per RECIST version 1.1 criteria - Participants must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 Exclusion Criteria: - Participants must not have active brain metastases or leptomeningeal metastases - Participants with HCC must not have any history of hepatic encephalopathy, any prior (within 1 year) or current clinically significant ascites - History of allergy or hypersensitivity to study drug components - Participants with serious or uncontrolled cardiovascular disease - Excluding patients with serious or uncontrolled medical disorders - Participants with a condition requiring systemic treatment with either corticosteroids (> 10 mg daily prednisone equivalent) or other immunosuppressive medications within 14 days of start of study treatment - Participants with an active, known, or suspected autoimmune disease - Participants must not have evidence of organ dysfunction or any clinically significant deviation from normal in physical examination, vital signs, ECG or clinical laboratory determinations beyond what is consistent with the target population 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

Have questions? Live support is available 24/7 - Call 855-907-3286 or email clinical.trials@bms.com

Have questions? Live support is available 24/7 -
Call 855-907-3286 or email clinical.trials@bms.com