To investigate and collect post-marketing data on the safety of Stivarga in real world practice in its registered indication(s) as required by Health Authority.
Study Type
OBSERVATIONAL
Enrollment
316
Patients treated by Physician with Stivarga under approved local prescriptions
Unnamed facility
Multiple Locations, South Korea
Percentage of patients with serious adverse events
Every 2 months (monthly safety assessment within first two cycles)
Time frame: Up to 30 days after terminating treatment
Percentage of patients with adverse drug reactions (ADRs)
Every 2 months (monthly safety assessment within first two cycles)
Time frame: Up to 30 days after terminating treatment
Overall response
Time frame: Up to 6 years
Progression free survival (PFS)
Time frame: Up to 6 years
Overall survival (OS)
Time frame: Up to 6 years
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