The purpose of this study is to determine if nivolumab added to the standard of care therapy (SOC) given after surgery is more effective than SOC alone in prolonging disease free survival in NSCLC participants with minimal residual disease detected after surgery.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Specified dose on specified days
Specified dose on specified days
Specified dose on specified days
Disease-free survival (DFS)
Time frame: Approximately 24 months
Circulating tumor DNA (ctDNA) response rate
Time frame: Approximately 36 months
ctDNA duration of response (DOR)
Time frame: Approximately 36 months
ctDNA time to response (TTR)
Time frame: Approximately 36 months
Incidence of adverse events (AEs)
Time frame: Approximately 36 months
Incidence of serious adverse events (SAEs)
Time frame: Approximately 36 months
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Specified dose on specified days
Specified dose on specified days
Specified dose on specified days
Specified dose on specified days
Specified dose on specified days
Observation by the investigator