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Adverse event reporting can be found at the bottom of the page.

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DUPIXENT®

(dupilumab) in uncontrolled Chronic Obstructive Pulmonary Disease

A breakthrough therapy in adults with uncontrolled chronic obstructive pulmonary disease (COPD) for MORE I CAN MOMENTS1 

TARGET

Two key drivers of type 2 inflammation

REDUCE

Moderate and severe exacerbations

IMPROVE

How patients breathe and feel

Indication

DUPIXENT is indicated in adults as add-on maintenance treatment for uncontrolled COPD characterised by raised blood eosinophils on a combination of an inhaled corticosteroid (ICS), a long-acting beta2-agonist (LABA), and a long-acting muscarinic antagonist (LAMA), or on a combination of a LABA and a LAMA if ICS is not appropriate.1

For additional information, please click here for the Summary of Product Characteristics.

 

ABBREVIATIONS
COPD, chronic obstructive pulmonary disease; ICS, inhaled corticosteroid; LABA, long‑acting beta2‑agonist; LAMA, long‑acting muscarinic antagonist; MOA, mechanism of action; MOD, mechanism of disease

REFERENCES

  1. DUPIXENT (dupilumab). Summary of Product Characteristics. 2025. Date last accessed: December 2025. 

MAT-XU-2502771 (v1.0) | December 2025

Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. Adverse events should also be reported to the Sanofi drug safety department on Tel: +44 (0) 800 0902 314. Alternatively, send via email to UK-drugsafety@sanofi.com