HEAD AND NECK CANCER
Conditions
Interventions
None listed
Sponsors
Bristol-Myers Squibb Ono Pharmaceutical CO.,LTD.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Recurrent/metastatic HNC patients with disease progression on or after a platinum-based therapy treated with nivolumab at least once from 01-Jul-2017 through 31-Dec-2017
Exclusion criteria
Exclusion criteria: History of participation in any clinical trials prior- or post-nivolumab treatment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Summary statistics for continuous outcomes will include mean, standard deviation, median,inter-quartile range, and range. Summary statistics for categorical or ordinal outcomes will include frequency and percentage. The primary analysis includes a description of actual usage of nivolumab and assessment of effectiveness and safety in which pre-specified immune-related adverse events (irAEs) identified | — |
Countries
Japan
Contacts
Public ContactJumpei Kamimito
Mebix, Inc Oncology Group
Outcome results
None listed