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BMS Active Not Yet Recruiting Study icon

Active, Not Recruiting

Trial ID CA209-234  |   NCT02847728

Pattern of Use and Safety/Effectiveness of Nivolumab in Routine Oncology Practice

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Sorry, this study is no longer accepting new participants, but is still ongoing.
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Summary

  • Male and Female Gender icon
  • 18+
    Age Range
  • BMS Active Not Yet Recruiting Study icon
    Active, Not Recruiting

Overview

This is an observational, multicenter study in participants treated with nivolumab for the approved indications of melanoma and Lung cancer in Australia, the EU, Switzerland, the United Kingdom (UK), and the United States (US). The targeted countries in the EU for study participation include Austria, Belgium, Czech Republic, France, Germany, Hungary, Italy, Poland, and Spain. Study objectives are to assess the safety experience, survival, adverse event management, and outcomes of adverse events associated with nivolumab in routine oncology care facilities.

Key Eligibility Criteria

Inclusion Criteria: - Age ≥18 - Histologically or cytologically confirmed diagnosis of melanoma (including uveal melanoma) or lung cancer - Treatment with commercial nivolumab for the first time, alone or in combination with ipilimumab, for the approved indications of nivolumab within 14 days before informed consent for this study OR in the case where treatment has not yet been initiated, documentation that the treatment strategy is determined before an informed consent to study participation, and treatment is initiated within 28 days after informed consent Exclusion Criteria: - Prior participation in a clinical trial within the past 4 weeks - Previously treated with anti-PD-1, anti-PD-L1, or anti-PD-L2 antibodies - Previously treated with anti-CTLA-4 for lung cancer - Current or pending participation in a clinical trial - Current or pending systemic treatment for cancer other than melanoma and lung cancer - Inability to comply with the study protocol

Treatment Options

Study Arms

ASSIGNED INTERVENTION

Study Arms

Single Arm Design

ASSIGNED INTERVENTION

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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