RecruitingNCT07380711

Long-term Real-world Study of Dupilumab in COPD : Patient Characteristics, Safety and Patient-reported Outcomes

Prospective and Retrospective Observational Real-world Study to Characterize Patients With COPD on Dupilumab Long-term Treatment, and Assess Safety and Patient Reported Outcomes


Sponsor

Sanofi

Enrollment

500 participants

Start Date

Jan 28, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

The OBS19236 is a retrospective and prospective, non-interventional observational study in COPD patients treated with dupilumab as part of routine clinical care. It will follow-up about 350 to 500 participants over 36 months in up to 50 sites in France.


Eligibility

Min Age: 18 Years

Inclusion Criteria4

  • Patients willing and able to sign informed consent for use of their pseudonymized clinical data within the present non-intervention study.
  • Adult patients.
  • Patients with uncontrolled Chronic Obstructive Pulmonary Disease (COPD) despite long-acting muscarinic antagonist (LAMA)/ Long-acting beta2-agonist (LABA)/ Inhaled Corticosteroid (ICS) (or LAMA/LABA if ICS are not appropriate) therapy and elevated blood eosinophils (a blood eosinophil count ≥ 300 cells/microL).
  • Patients newly initiated on dupilumab treatment as indicated in the dupilumab summary of product characteristics (SmPC) in the specified label for COPD, determined by the treating physician, and independent of participation in the non-interventional study (NIS).

Exclusion Criteria4

  • Patient not eligible for dupilumab treatment according to SmPC.
  • Participation in an ongoing interventional study or participation in an interventional study up to 12 months before enrolment that might, in the treating physician's opinion, influence the assessments for the current study.
  • Any acute or chronic condition that, in the treating physician's opinion, would limit the patient's ability to complete questionnaires or to participate in this study or impact the interpretation of the results.
  • The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Locations(20)

Investigational Site Number : 2500021

Aix-en-Provence, France

Investigational Site Number : 2500043

Blois, France

Investigational Site Number : 2500044

Brest, France

Investigational Site Number : 2500009

Colmar, France

Investigational Site Number : 2500022

Juan-les-Pins, France

Investigational Site Number : 2500020

Le Chesnay, France

Investigational Site Number : 2500038

Libourne, France

Investigational Site Number : 2500033

Lyon, France

Investigational Site Number : 2500024

Marseille, France

Investigational Site Number : 2500002

Montpellier, France

Investigational Site Number : 2500047

Morlaix, France

Investigational Site Number : 2500040

Niort, France

Investigational Site Number : 2500026

Nîmes, France

Investigational Site Number : 2500017

Paris, France

Investigational Site Number : 2500001

Pessac, France

Investigational Site Number : 2500034

Pierre-Bénite, France

Investigational Site Number : 2500048

Saint-Pierre, France

Investigational Site Number : 2500029

Toulouse, France

Investigational Site Number : 2500010

Vantoux, France

Investigational Site Number : 2500035

Villeurbanne, France

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NCT07380711


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