The purpose of this study is to evaluate the safety, tolerability, compliance and mechanism of action of study drug (QBKPN SSI) in subjects with two or more second primary pre-invasive or invasive adenocarcinoma following surgical section of Stage 1 NSCLC.
Please refer to summary above.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
6
QBKPN SSI is administered subcutaneously for 12 weeks
BC Cancer Research Centre
Vancouver, Canada
Safety, tolerability and compliance variables
Assess the number of adverse events and subject reported data
Time frame: 16 weeks
Exploratory variables
Assess and identify biomarkers associated with immune response
Time frame: 16 weeks
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