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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT02847728
Registration number
NCT02847728
Ethics application status
Date submitted
28/06/2016
Date registered
28/07/2016
Date last updated
3/06/2024
Titles & IDs
Public title
Pattern of Use and Safety/Effectiveness of Nivolumab in Routine Oncology Practice
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Scientific title
Pattern of Use and Safety/Effectiveness of Nivolumab in Routine Oncology Practice
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Secondary ID [1]
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CA209-234
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Melanoma
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Lung Cancer
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Condition category
Condition code
Cancer
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Malignant melanoma
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Intervention/exposure
Study type
Observational
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Single Arm Design - The study encompasses a single arm design with 417 adults treated with nivolumab for histologically or cytologically confirmed melanoma and 772 adults treated with nivolumab for histologically or cytologically confirmed lung cancer.
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Incidence rate of and severity of immune-related pneumonitis - Melanoma
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Assessment method [1]
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Timepoint [1]
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up to nine years
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Primary outcome [2]
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Incidence rate of and severity of immune-related colitis- Melanoma
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Assessment method [2]
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0
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Timepoint [2]
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up to nine years
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Primary outcome [3]
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Incidence rate of and severity of immune-related hepatitis - Melanoma
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Assessment method [3]
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0
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Timepoint [3]
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up to nine years
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Primary outcome [4]
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Incidence rate of and severity of immune-related nephritis/renal dysfunction - Melanoma
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Assessment method [4]
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0
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Timepoint [4]
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up to nine years
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Primary outcome [5]
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Incidence rate of and severity of immune-related endocrinopathies - Melanoma
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Assessment method [5]
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0
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Timepoint [5]
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up to nine years
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Primary outcome [6]
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Incidence rate of and severity of immune-related rash (including toxic epidermal necrolysis) - Melanoma
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Assessment method [6]
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0
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Timepoint [6]
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up to nine years
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Primary outcome [7]
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Incidence rate of and severity of other immune-related adverse events (eg, uveitis, pancreatitis, demyelination, Guillain-Barre Syndrome, myasthenic syndrome, and encephalitis) - Melanoma
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Assessment method [7]
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Timepoint [7]
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up to nine years
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Primary outcome [8]
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Incidence rate of and severity of severe infusion reactions- Melanoma
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Assessment method [8]
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0
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Timepoint [8]
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up to nine years
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Primary outcome [9]
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Incidence rate of and severity of immune-related pneumonitis - Lung Cancer
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Assessment method [9]
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0
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Timepoint [9]
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up to nine years
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Primary outcome [10]
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Incidence rate of and severity of immune-related colitis - Lung Cancer
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Assessment method [10]
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0
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Timepoint [10]
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up to nine years
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Primary outcome [11]
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Incidence rate of and severity of immune-related hepatitis - Lung Cancer
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Assessment method [11]
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Timepoint [11]
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up to nine years
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Primary outcome [12]
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Incidence rate of and severity of immune-related nephritis/renal dysfunction - Lung Cancer
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Assessment method [12]
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0
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Timepoint [12]
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up to nine years
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Primary outcome [13]
0
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Incidence rate of and severity of immune-related endocrinopathies - Lung Cancer
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Assessment method [13]
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0
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Timepoint [13]
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up to nine years
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Primary outcome [14]
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0
Incidence rate of and severity of other immune related adverse events (eg, uveitis, pancreatitis, demyelination, Guillain-Barre Syndrome, myasthenic syndrome, and encephalitis) - Lung Cancer
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Assessment method [14]
0
0
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Timepoint [14]
0
0
up to nine years
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Primary outcome [15]
0
0
Incidence rate of and severity of severe infusion reactions - Lung Cancer
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Assessment method [15]
0
0
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Timepoint [15]
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0
up to nine years
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Primary outcome [16]
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0
Incidence rate of and severity of immune-related rash (including toxic epidermal necrolysis), - Lung Cancer
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Assessment method [16]
0
0
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Timepoint [16]
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up to nine years
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Secondary outcome [1]
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Adverse Events
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Assessment method [1]
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Other nivolumab treatment-related AEs
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Timepoint [1]
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Up to nine years
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Secondary outcome [2]
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Management of Immune-related AEs:
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Assessment method [2]
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0
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Timepoint [2]
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Up to nine years
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Secondary outcome [3]
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Outcomes of Immune-related AEs:
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Assessment method [3]
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0
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Timepoint [3]
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Up to nine years
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Secondary outcome [4]
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Overall Survival:
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Assessment method [4]
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1-, 2-, 3-, 4-, and 5-year overall and median survival
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Timepoint [4]
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Up to nine years
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Secondary outcome [5]
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Nivolumab treatment pattern
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Assessment method [5]
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Timepoint [5]
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Up to nine years
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Eligibility
Key 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
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key 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
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Study design
Purpose
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Duration
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Selection
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Timing
Prospective
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
28/07/2016
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
31/03/2024
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Sample size
Target
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Accrual to date
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Final
1189
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Recruitment in Australia
Recruitment state(s)
NSW,VIC,WA
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Recruitment hospital [1]
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Local Institution - 1001 - Lismore
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Recruitment hospital [2]
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Local Institution - 1002 - Wagga Wagga
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Recruitment hospital [3]
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Local Institution - 1006 - Franskton
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Recruitment hospital [4]
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Local Institution - 1003 - Wodonga
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Recruitment hospital [5]
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Local Institution - 1005 - Subiaco
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Recruitment postcode(s) [1]
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2480 - Lismore
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Recruitment postcode(s) [2]
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2650 - Wagga Wagga
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Recruitment postcode(s) [3]
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3199 - Franskton
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Recruitment postcode(s) [4]
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3690 - Wodonga
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Recruitment postcode(s) [5]
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6008 - Subiaco
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Recruitment outside Australia
Country [1]
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United States of America
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California
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United States of America
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Florida
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United States of America
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Illinois
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United States of America
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Louisiana
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United States of America
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Mississippi
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United States of America
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Missouri
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United States of America
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New Jersey
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United States of America
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Pennsylvania
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United States of America
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South Carolina
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United States of America
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Texas
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Austria
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Innsbruck
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Austria
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Klagenfurt Am Woerthersee
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Austria
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State/province [13]
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Krems an der Donau
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Belgium
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State/province [14]
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Antwerpen
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Belgium
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Kortrijk
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Belgium
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Namur
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Czechia
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Olomouc
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France
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Lyon
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France
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Metz-Tessy
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France
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Nancy
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France
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Saint Jean Priest En Jarez
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France
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Toulouse
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France
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Vandoeuvre-les-Nancy
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Germany
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Baden-Württemberg
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Germany
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Rheinland Pfa
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Sachsen-Anhalt
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Germany
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Schleswig-Holstein
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Germany
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Augsburg
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Ballenstedt
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Berlin
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Bochum
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Ulm
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Strathclyde
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United Kingdom
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Bristol
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Bristol-Myers Squibb
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
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.
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Trial website
https://clinicaltrials.gov/study/NCT02847728
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Bristol-Myers Squibb
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Address
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Bristol-Myers Squibb
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Address
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Phone
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Email
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Contact person for scientific queries
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT02847728
Download to PDF