non-small cell lung cancer
Conditions
Interventions
None listed
Sponsors
Chugai Pharmaceutical Co. Ltd.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: All patients who are scheduled to receive TECENTRIQ at contracted institutions during this surveillance's enrollment period.
Exclusion criteria
Exclusion criteria: No criteria
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The incidence of ADRs. | — |
Secondary
| Measure | Time frame |
|---|---|
| - The time of onset of ADRs. - The treatment status and outcome of ADRs. - The incidence of ADRs for each patient baseline characteristic. | — |
Countries
Japan
Contacts
Public ContactAyaka Shimizu
Chugai Pharmaceutical Co. Ltd. Real world data science Dept.
Outcome results
None listed