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NCT06418412

A Pan-Asian Clinical Database of EGFR Exon 20 Insertion Mutated NSCLC

Recruiting · Not specified · National Cancer Centre, Singapore · registry updated 2025-06-12

Inclusion and exclusion lines below are quoted from ClinicalTrials.gov. No match score is shown, because a score needs a person's age, biomarkers, and treatment dates. Confirm the record with the study team.

There are limited in depth studies on the epidemiology and clinical management of EGFR exon 20 insertion mutated NSCLC in Asia. In addition, there is preliminary data suggesting the exact location of the insertion and variant may influence the response and efficacy to novel EGFR targeted therapies. This study aims to fill this knowledge gap, by comprehensively characterising the epidemiology and clinical outcomes of Asian advanced EGFR exon 20 insertion mutated NSCLC patients.

Inclusion

  • Histologically confirmed advanced NSCLC
  • Positive testing result from any locally approved test (including but not limited to RT-PCR, Cobas and NGS) for EGFR exon 20 insertion mutation
  • Diagnosis date from 1 Jan 2013 to 31 Dec 2024 (to allow for minimum 12 months of follow-up clinical and treatment outcome data)
  • Male or female adults, age as defined by local regulations

Exclusion

  • \. Patients without an EGFR exon 20 insertion mutation

Open NCT06418412 on ClinicalTrials.govAll conditions

A Pan-Asian Clinical Database of EGFR Exon 20 Insertion Mutated NSCLC | Clinical Trial Matcher