Status: Recommended with restrictions | ||
Dupilumab (Dupixent®) is recommended as an option for restricted use within NHS Wales. Dupilumab (Dupixent®) is licensed in children 6 to 11 years old as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (FeNO), who are inadequately controlled with medium to high dose inhaled corticosteroids (ICS) plus another medicinal product for maintenance treatment. Dupilumab (Dupixent®) is restricted for use in a subpopulation of the licensed indication in line with the National Institute of Health and Care Excellence recommendation for the restricted use of dupilumab for treating severe asthma with type 2 inflammation (TA751). Dupilumab (Dupixent®) is not recommended for use within NHS Wales outside of this subpopulation. This recommendation applies only in circumstances where the approved Patient Access Scheme (PAS) is utilised or where the list/contract price is equivalent or lower than the PAS price. |
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Medicine details |
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Medicine name | dupilumab (Dupixent®) | |
Formulation | 200 mg solution for injection, 300 mg solution for injection | |
Reference number | 4017 | |
Indication | Indicated in children 6 to 11 years old as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (FeNO) who are inadequately controlled with medium to high dose inhaled corticosteroids (ICS) plus another medicinal product for maintenance treatment |
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Company | Sanofi-Aventis Ltd | |
BNF chapter | Respiratory system | |
Submission type | Licence extension for paediatric use | |
Status | Recommended with restrictions | |
Advice number | 1522 | |
AWMSG meeting date | 14/09/2022 | |
Date of issue | 03/10/2022 | |
Commercial arrangement | PAS | |
Further information |