This study is part of the development and validation of a non-invasive lung screening test which aim to identify early stage lung cancer in patients at high risk for lung cancer.
This is a prospective, case-control, multi-center, observational nonsignificant risk study. The study aims to collect blood and clinical data from subjects undergoing Low Dose CT (LDCT) for lung cancer screening and subjects with confirmed lung cancer.
Study Type
OBSERVATIONAL
Enrollment
5,000
Peripheral blood will be collected via routine venipuncture procedure
Collection of blood samples
Collect blood to support the development and validation of a multi analyte test for lung cancer screening
Time frame: 24 Months
Clinical data collection
Collect clinical data to support the development and validation of a multi analyte test for lung cancer screening
Time frame: 24 Months
Performance
Performance of the assay in terms of (1) Sensitivity (2) Specificity (3) NPV (negative predictive value) and (4) PPV (positive predictive value)
Time frame: 36 Months
Sensitivity
Performance of the assay in terms of Sensitivity
Time frame: 36 Months
Specificity
Performance of the assay in terms of Specificity
Time frame: 36 Months
Negative Predictive Value
Performance of the assay in terms of NPV (negative predictive value)
Time frame: 36 Months
Positive Predictive Value
Performance of the assay in terms of PPV (positive predictive value)
Time frame: 36 Months
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