Study identifier:D5162L00064
ClinicalTrials.gov identifier:NCT07613424
EudraCT identifier:N/A
CTIS identifier:N/A
A Multicenter, Prospective Study of MET Concordance and Gene Profiling in First-line Non-small Cell Lung Cancer (NSCLC) (Genomet)
Non-small Cell Lung Cancer
N/A
No
-
All
1000
Interventional
18 Years - n/a
Allocation: Non-randomized
Endpoint Classification: -
Intervention Model: Parallel Assignment
Masking: -
Primary Purpose: Basic Science
Verified 01 Jun 2026 by AstraZeneca
AstraZeneca
-
No locations available
| Arms | Assigned Interventions |
|---|---|
| Other: cohort 1 Participants will be assigned to study cohorts based on the EGFR mutation status determined by central NGS testing. Only participants with EGFR mutations (EGFR 19del+/L858R+) will be included in Cohort 1. | Diagnostic Test: NGS testing NGS testing first for all participants and then cohort assignment for each participant can be derived based on NGS results. Diagnostic Test: MET IHC testing the participants of cohort 1 need to do MET IHC testing. |
| Other: cohort 2 Participants will be assigned to study cohorts based on the EGFR mutation status determined by central NGS testing.Those with no actionable genomic alterations (non-AGA), defined as EGFR 19del-/L858R-/20ins-/PACC-, ALK-, ROS1-, BRAF V600-, NTRK-, KRAS G12C-, MET amp-, MET exon14-, and RET-, will be assigned to Cohort 2. | Diagnostic Test: NGS testing NGS testing first for all participants and then cohort assignment for each participant can be derived based on NGS results. Diagnostic Test: PD-L1 and Her2 testing the participants of cohort 1 need to do PD-L1 and Her2 testing. |
| Other: cohort 3 Participants will be assigned to study cohorts based on the EGFR mutation status determined by central NGS testing.Those with other actionable genomic alterations (AGA, excluding EGFR 19del+/L858R+), defined as EGFR 20ins+, EGFR PACC+, ALK+, ROS1+, BRAF V600+, NTRK+, KRAS G12C+, MET amp+, MET exon14+, or RET+, will be assigned to Cohort 3. | Diagnostic Test: NGS testing NGS testing first for all participants and then cohort assignment for each participant can be derived based on NGS results. |