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Active, Not Recruiting

A Study of Nivolumab in Advanced Non-Small Cell Lung Cancer (NSCLC) - CA209-370

Updated: 1 July, 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 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 2

    Phase

  • Gender(s)

  • 18+

    Age Range

  • Active, Not Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
Experimental: Group A Nivolumab
Drug: Nivolumab
Experimental: Group A Nivolumab + SOC maintenance therapy
Drug: Bevacizumab Drug: Pemetrexed Drug: Nivolumab
Active Comparator: Group A SOC maintenance therapy
Drug: Bevacizumab Drug: Pemetrexed
Other: Group B Best supportive care
Other: Best Supportive Care
Experimental: Group B Nivolumab
Drug: Nivolumab
Active Comparator: Group C Investigator's choice chemotherapy
Drug: nab-Paclitaxel Drug: Pemetrexed Drug: Docetaxel Drug: Carboplatin Drug: Gemcitabine Drug: Paclitaxel
Experimental: Group C Nivolumb
Drug: Nivolumab
Active Comparator: Group D Erlotinib
Drug: Erlotinib
Experimental: Group D Nivolumab + Erlotinib
Drug: Nivolumab Drug: Erlotinib
Experimental: Group E Nivolumab + Crizotinib
Drug: Nivolumab Drug: Crizotinib

Key Eligibility Criteria

For more information regarding BMS clinical trial participation, please visit www.BMSStudyConnect.com Inclusion Criteria: - Histologically confirmed locally advanced or stage IV NSCLC - Eastern Cooperative Oncology Group (ECOG) Performance status (PS) 0-2 - Tumor tissue sections must be available for biomarker evaluation Exclusion Criteria: - Untreated or active/progressing Central Nervous system (CNS) metastases - Active, known or suspected autoimmune disease - Known history of testing positive for HIV or AIDS - Active or chronic infection of hepatitis B virus or hepatitis C

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