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Active, Not Recruiting

Risk Factors and Outcomes of Immune-Mediated Encephalitis Following Exposure to Nivolumab - CA209-567

Updated: 10 January, 2018   |   ClinicalTrials.gov

Print Friendly Summary

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Trial Details

  • Gender(s)

  • N/A

    Age Range

  • Active, Not Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
Patients Treated with Nivolumab followed by Encephalitis Event
Biological: Nivolumab

Key Eligibility Criteria

Inclusion Criteria: - Moderate, severe, life-threatening or fatal encephalitis events occurring in patients treated with nivolumab and reported to the Sponsor Exclusion Criteria: - Encephalitis cases identified through literature reviews and not reported to the Sponsor - Encephalitis cases identified from company-sponsored observational studies with secondary data collection - Spontaneous reports not submitted directly to the Sponsor 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