UmbREALung - A Retrospective and Prospective, Observational, Real World Multi-cohort Study of Patients With Non-small Cell Lung Cancer (NSCLC) Initiating Approved Drugs Developed by AZ or as Part of an AZ Alliance
NCT ID: NCT06726720
Last Updated: 2026-01-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
300 participants
OBSERVATIONAL
2024-12-16
2032-06-30
Brief Summary
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Patients will be enrolled in the study if they have received (retrospective), receive (retrospective and prospective) or will receive (prospective) approved drugs developed by AZ or as part of an AZ alliance according to the eligibility criteria.
Treatment plan and decision are made independently by each treating physician prior to inclusion in this study.
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Detailed Description
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Conditions
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Study Design
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COHORT
OTHER
Study Groups
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Cohort 1 - Resectable
Ambispective, observational, study of patients with non-small cell lung cancer initiating approved drugs developed by AZ or as part of an AZ alliance in resectable NSCLC
No interventions assigned to this group
Cohort 2 - Unresectable
Ambispective, observational, study of patients with non-small cell lung cancer initiating approved drugs developed by AZ or as part of an AZ alliance in Unresectable NSCLC
No interventions assigned to this group
Cohort 3 - Metastatic
Ambispective, observational, study of patients with non-small cell lung cancer initiating approved drugs developed by AZ or as part of an AZ alliance in Metastatic NSCLC
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Patients with histologically or cytologically proven NSCLC
* Patients initiated with approved drugs developed by AZ or as part of an AZ alliance at the time of the enrollment or within the previous three weeks.
* Informed patients who consent to participate in the study as per local regulations.
Exclusion Criteria
\* with the exception on low-interventional studies (RIPH2) where the intervention does not involve the NSCLC treatment
* Patients already enrolled in another module of the cohort in UMBREALUNG
* Patients under safeguard of justice, curatorship or guardianship
18 Years
ALL
No
Sponsors
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AstraZeneca
INDUSTRY
Responsible Party
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Locations
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Research Site
Aix-en-Provence, , France
Research Site
Angers, , France
Research Site
Aurillac, , France
Research Site
Auxerre, , France
Research Site
Avignon, , France
Research Site
Blois, , France
Research Site
Bordeaux, , France
Research Site
Bourg-en-Bresse, , France
Research Site
Carcassonne, , France
Research Site
Chalon-sur-Saône, , France
Research Site
Chambéry, , France
Research Site
Châteauroux, , France
Research Site
Créteil, , France
Research Site
Dieppe, , France
Research Site
Dinan, , France
Research Site
Dreux, , France
Research Site
Epagny Metz Tessy, , France
Research Site
Le Coudray, , France
Research Site
Limoges, , France
Research Site
Lyon, , France
Research Site
Marseille, , France
Research Site
Meaux, , France
Research Site
Metz, , France
Research Site
Mulhouse, , France
Research Site
Nancy, , France
Research Site
Nantes, , France
Research Site
Neuilly-sur-Seine, , France
Research Site
Nice, , France
Research Site
Nîmes, , France
Research Site
Perpignan, , France
Research Site
Saint-Brieuc, , France
Research Site
Saint-Etienne, , France
Research Site
Saint-Herblain, , France
Research Site
Suresnes, , France
Research Site
Toulouse, , France
Research Site
Troyes, , France
Research Site
Valenciennes, , France
Research Site
Vannes, , France
Research Site
Villefranche-sur-Saône, , France
Research Site
Villeurbanne, , France
Countries
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Central Contacts
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Other Identifiers
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D4191R00060
Identifier Type: -
Identifier Source: org_study_id
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