Study identifier:D133FR00204
ClinicalTrials.gov identifier:NCT06245837
EudraCT identifier:N/A
CTIS identifier:N/A
Multicenter, non-interventional, observational study of treatment and biomarker testing patterns, treatment outcomes in advanced/metastatic NSCLC with and without actionable genomic alterations in routine clinical practice in Russia
Non-small-cell lung cancer
N/A
No
-
All
1500
Observational
n/a - n/a
Allocation: N/A
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Feb 2025 by AstraZeneca
AstraZeneca
-
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
Location
Status
Location
Perm, Russian Federation
Status
Recruiting
Location
Ufa, Russian Federation
Status
Recruiting
Location
Moscow, Russian Federation
Status
Recruiting
Location
Moscow, Russian Federation
Status
Withdrawn
Location
Rostov-on-Don, Russian Federation
Status
Withdrawn
Location
Saint-Petersburg, Russian Federation
Status
Recruiting
Location
Arkhangelsk, Russian Federation
Status
Recruiting
Location
Yaroslavl, Russian Federation
Status
Recruiting
Arms | Assigned Interventions |
---|
This information is not intended to replace the informed medical advice or medical treatments of a healthcare professional. Only a physician can determine if a specific medicine is the correct treatment for a particular patient. If you have questions regarding any information contained in this site, you must consult a suitably qualified healthcare professional. Before prescribing any AstraZeneca products, Healthcare Professionals should view their country specific information.