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

Results pending

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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Recruitment Status

RECRUITING

Total Enrollment

300 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-12-16

Study Completion Date

2032-06-30

Brief Summary

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This is an ambispective, observational, multicenter and multicohort study, targeting patients with NSCLC initiating approved drugs developed by AZ or as part of an AZ alliance, in the participating countries, as monotherapy or in combination at any stage of disease. Three cohorts are designed, based on the stage of NSCLC (resectable, unresectable and metastatic). The multicohort study is modular in design. Specific modules will be set up separately to assess each new indication of drugs developed by AZ or as part of an AZ alliance once European marketing authorization (MA) has been granted and made available in the participating countries.

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.

Detailed Description

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Conditions

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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

Study Design

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Observational Model Type

COHORT

Study Time Perspective

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

* Adult patients (≥ 18 years old)
* 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

* Patients participating in an interventional clinical trial for NSCLC\*

\* 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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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AstraZeneca

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Research Site

Aix-en-Provence, , France

Site Status RECRUITING

Research Site

Angers, , France

Site Status RECRUITING

Research Site

Aurillac, , France

Site Status RECRUITING

Research Site

Auxerre, , France

Site Status NOT_YET_RECRUITING

Research Site

Avignon, , France

Site Status RECRUITING

Research Site

Blois, , France

Site Status RECRUITING

Research Site

Bordeaux, , France

Site Status NOT_YET_RECRUITING

Research Site

Bourg-en-Bresse, , France

Site Status RECRUITING

Research Site

Carcassonne, , France

Site Status RECRUITING

Research Site

Chalon-sur-Saône, , France

Site Status RECRUITING

Research Site

Chambéry, , France

Site Status RECRUITING

Research Site

Châteauroux, , France

Site Status NOT_YET_RECRUITING

Research Site

Créteil, , France

Site Status RECRUITING

Research Site

Dieppe, , France

Site Status RECRUITING

Research Site

Dinan, , France

Site Status RECRUITING

Research Site

Dreux, , France

Site Status NOT_YET_RECRUITING

Research Site

Epagny Metz Tessy, , France

Site Status NOT_YET_RECRUITING

Research Site

Le Coudray, , France

Site Status RECRUITING

Research Site

Limoges, , France

Site Status RECRUITING

Research Site

Lyon, , France

Site Status RECRUITING

Research Site

Marseille, , France

Site Status RECRUITING

Research Site

Meaux, , France

Site Status RECRUITING

Research Site

Metz, , France

Site Status RECRUITING

Research Site

Mulhouse, , France

Site Status RECRUITING

Research Site

Nancy, , France

Site Status RECRUITING

Research Site

Nantes, , France

Site Status RECRUITING

Research Site

Neuilly-sur-Seine, , France

Site Status NOT_YET_RECRUITING

Research Site

Nice, , France

Site Status RECRUITING

Research Site

Nîmes, , France

Site Status NOT_YET_RECRUITING

Research Site

Perpignan, , France

Site Status RECRUITING

Research Site

Saint-Brieuc, , France

Site Status RECRUITING

Research Site

Saint-Etienne, , France

Site Status RECRUITING

Research Site

Saint-Herblain, , France

Site Status RECRUITING

Research Site

Suresnes, , France

Site Status RECRUITING

Research Site

Toulouse, , France

Site Status RECRUITING

Research Site

Troyes, , France

Site Status NOT_YET_RECRUITING

Research Site

Valenciennes, , France

Site Status RECRUITING

Research Site

Vannes, , France

Site Status RECRUITING

Research Site

Villefranche-sur-Saône, , France

Site Status RECRUITING

Research Site

Villeurbanne, , France

Site Status RECRUITING

Countries

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France

Central Contacts

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AstraZeneca Clinical Study Information Center

Role: CONTACT

1-877-240-9479

Other Identifiers

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D4191R00060

Identifier Type: -

Identifier Source: org_study_id

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