Prospective External Control Cohort In Patients With Newly Diagnosed Advanced or Metastatic EGFR Mutant Non-Small Cell Lung Cancer
Sponsored by N-Power Medicine
About this study
The objective of this study is to build a prospective cohort in patients with locally advanced or metastatic NSCLC with common EGFR mutations. In NPM-002, there will be standardized data collection at baseline, on-treatment and at discontinuation of therapy. Patients who enroll prior to initiation of osimertinib treatment (\~30%) will undergo imaging with standardized intervals.
Where this study is enrolling (10)
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Torrance Memorial Physician Network-Cancer Care
Torrance, California
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Pacific Cancer Care
Monterey, California
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John Muir Health
Walnut Creek, California
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Bayhealth Cancer Center- Kent
Dover, Delaware
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Bayhealth Cancer Center- Sussex
Milford, Delaware
Show all 10 locations
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Kootenai Clinic Cancer Services Coeur d'Alene
Coeur d'Alene, Idaho
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Northwest Oncology & Hematology
Elk Grove Village, Illinois
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New Mexico Oncology Hematology Consultants
Albuquerque, New Mexico
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Lankenau Medical Center
Paoli, Pennsylvania
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Oncology Consultants, P.A.
Houston, Texas
Who can participate
Inclusion criteria
- ✓Be ≥18 years of age at the time of informed consent
- ✓Evidence of a confirmed diagnosis of EGFR mutant (EGFR exon 19del or EGFR exon 21 L858R) locally advanced or metastatic NSCLC diagnosed on Jan 1st 2024 or later.
Exclusion criteria
- ✕ECOG≥2 at diagnosis of advanced or metastatic NSCLC
- ✕Evidence of prior treatment with osimertinib, amivantamab or lazertinib. For the planned selection and analysis of external controls, further eligibility criteria will be applied according to the COPERNICUS SAP.
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Completing a questionnaire on Clinably does not enroll you in a clinical trial or confirm your eligibility. Only the research team can determine whether you qualify to participate. These results are based on the information you provide and are intended to help you start a conversation with the research team.
Trial data sourced from ClinicalTrials.gov.