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Treatment and Biomarker Testing Patterns,Treatment Outcomes in a/m NSCLC With and Without Actionable Genomic Alterations

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AstraZeneca

Status

Active, not recruiting

Conditions

Non-small-cell Lung Cancer

Study type

Observational

Funder types

Industry

Identifiers

NCT06245837
D133FR00204

Details and patient eligibility

About

Planned study population consists of approximately 1500 adult patients with a/m NSCLC in Russia, in about 20 oncological centers (in each center it is expected to recruit about 75 patients) in different regions of Russia in order to provide representative study sample

Enrollment

1,500 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Morphologically confirmed NSCLC with or without actionable genomic alterations (AGA, i.e. EGFR, ALK, ROS1, NTRK, BRAF, MET exon 14 skipping, RET, ERBB2 (HER2), or KRAS)
  2. Age ≥18 years at the time of NSCLC diagnosis;
  3. Locally advanced or metastatic disease defined as incident stage IIIB/IIIC/IV NSCLC or stage I-IIIA then progressed to stage IIIB-IV disease and not eligible for curative-intent treatment (the date of progression is included in the database);
  4. Available data on at least one line of systemic therapy for advanced/metastatic disease within the period since January 2022 until January 2025;
  5. Patients may be alive or deceased at the time of medical record abstraction

Exclusion criteria

  1. Patients participated or participating in clinical trials or any early access program within period since the index date until the end of study period;
  2. Diagnosis of another cancer (except for melanoma/skin cancer) at or within 5 years prior to NSCLC diagnosis or any ongoing systemic anti-cancer therapy regimen at the time of NSCLC diagnosis

Trial contacts and locations

16

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Central trial contact

AstraZeneca Clinical Study Information Center

Data sourced from clinicaltrials.gov

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