this is a phase I study comparing PK similarity of sintilimab by different production process (approved versus M1b) in Chinese advanced or metastatic NSCLC patients who have failed or been intolerant to at least one prior line of standard treatment
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
48
Intravenous infusion
Intravenous infusion
The First Affiliated Hospital of Bengbu Medical College
Bengbu, China
PK is defined as AUC0-∞.
Time frame: 28 days
PK is defined as Cmax.
Time frame: 28 days
Safety of sintilimab (approved) versus sintilimab (M1b). AE is defined as treatment-related adverse events assessed by CTCAE v5.0.
Time frame: from randomization through 90 days after last dosing
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