This will be a single-arm, multicenter, prospective, observational, real-world study and the data source is the patients' medical record at each site. A total of 78 patients will be enrolled in the study.
Study Type
OBSERVATIONAL
Enrollment
78
IMFINZI
Frequency and proportion of patients with Grade 3/4 possibly related adverse events (PRAEs)*
\- Frequency and proportion of patients with Grade 3/4 possibly related adverse events (PRAEs)\*
Time frame: 21 months
Frequency and proportion of patients with treatment emergent adverse events (TEAE) & serious adverse events (SAEs), , mortality.
Frequency and proportion of patients with treatment emergent adverse events (TEAE) \& serious adverse events (SAEs), , mortality.
Time frame: 21 months
Time to occurrence of first AEs and first SAEs
Time to occurrence of first AEs and first SAEs
Time frame: 21 months
* PRAEs as assessed per the WHO-UMC criteria
\* PRAEs as assessed per the WHO-UMC criteria
Time frame: 21 months
AstraZeneca Clinical Study Information Center
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