About this trial
The purpose of this multi-national disease registry is to collect prospectively (with longitudinal follow-up) high-quality, standardized, and contemporaneous data to capture changes in the non-small cell lung cancer (NSCLC) treatment landscape and outcomes over time.
The registry will capture data on participants; demographic, clinical characteristics (including biomarker data), treatment patterns, and effectiveness and safety outcomes for advanced NSCLC with mesenchymal-epithelial transition exon 14(METex14) participants treated with systemic therapy.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Participants who signed ICF
Participants with advanced stage (stages IIIB-IV) NSCLC (all histologies) and Confirmed METex14 skipping alterations (by valid assay)
Participants who are starting or are already being treated with systemic therapy
Disqualifiers
Participants who are enrolled in a clinical trial
Trial population
Participants with advanced stage (stages IIIB-IV) NSCLC and confirmed METex14 skipping alterations who are initiating or already treated with a systemic therapy will be included.
Trial design
Other
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Best Overall Response (BOR)
Tumor Response According to Response Evaluation Criteria in Solid Tumors Version (RECIST) 1.1
Overall Survival (OS)
Number of Participants with Adverse Events (AEs)
Sponsors and contacts
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EMD Serono Research & Development Institute, Inc.
Lead sponsor
Merck KGaA, Darmstadt, Germany
Collaborator