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DUPIXENT®

(dupilumab) in uncontrolled Chronic Obstructive Pulmonary Disease

Mechanism of Action

Indication

DUPIXENT is indicated in adults as add-on maintenance treatment for uncontrolled COPD characterised by raised blood eosinophils on a combination of an ICS, a LABA, and a LAMA, or on a combination of a LABA and a LAMA if ICS is not appropriate.1

Please refer to the Summary of Product Characteristics for further information.1

Dupixent is the first biologic to target type 2 inflammation in COPD1

Interleukin (IL)-4 and IL-13 are key and central cytokines of type 2 inflammation2,3

il4- cytokine

IL-4 perpetuates underlying type 2 inflammation by differentiating naïve T cells into T helper 2 cells.3

IL-13 promotes goblet cell hyperplasia and mucus hypersecretion.3

Local Inflammation3 -7

  • Mucus hypersecretion
  • Airway remodeling
  • Airway smooth muscle hypertrophy
  • Epithelial barrier dysfunction
  • Parenchymal destruction
     

Systemic Inflammation3,5

  • Eosinophil trafficking
  • B-cell class switching
  • Mast cell degranulation

  • Dyspnoea
  • Cough
  • Sputum production

Through dual inhibition of IL-4 and IL-13 signalling, DUPIXENT used in combination with triple inhaled therapy, or double inhaled therapy if ICS is not appropriate, demonstrated an improvement in symptoms1,9–11

ABBREVIATIONS
COPD, chronic obstructive pulmonary disease; ICS, inhaled corticosteroid; IL, interleukin; SOC, standard of care

REFERENCES

  1.  DUPIXENT (dupilumab). Summary of Product Characteristics. 2025. Date last accessed: December 2025.
  2. Garudadri S, Woodruff PG. Ann Am Thorac Soc. 2018;15(Suppl 4):S234‑S238.
  3. Gandhi NA, et al. Nat Rev Drug Discov. 2016;15(1):35‑50.
  4. Rabe KF,  et al. Am J Respir Crit Care Med. 2023;208(4):395-405.
  5. Wouters EF, et al. Proc Am Thorac Soc. 2009;6:638‑647.
  6. Saatian B, et al. Tissue Barriers. 2013;1(2):e24333.
  7. Cooper PR, et al. Am J Respir Cell Mol Biol. 2010;43(2):220‑226.
  8. Global Initiative for Chronic Obstructive Lung Disease. Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease (2025 report). Available at: https://goldcopd.org/2025-gold-report/ Date last accessed: December 2025.
  9. Bhatt SP, et al. N Engl J Med. 2023;389(3):205‑214.
  10. Bhatt SP, et al. N Engl J Med. 2024;390(24):2274‑2283.
  11. Bhatt SP, et al. Lancet Respir Med. 2025;13:234‑243.

MAT-XU-2503518 (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