Following a limited submission
AWMSG advice |
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| Status: Recommended with restrictions | |||
Dupilumab (Dupixent®) is recommended as an option for restricted use within NHS Wales. Dupilumab (Dupixent®) is licensed for the treatment of moderate-to-severe atopic dermatitis in adolescents ≥ 12 to < 18 years who are candidates for systemic therapy. Dupilumab (Dupixent®) is restricted for the treatment of moderate-to-severe atopic dermatitis in adolescents ≥ 12 to < 18 years who are candidates for systemic therapy, only if the disease has not responded to at least one other systemic therapy, or these are contraindicated or not tolerated. 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 | 300 mg solution for injection and 200 mg solution for injection | ||
| Reference number | 4089 | ||
| Indication | Treatment of moderate-to-severe atopic dermatitis in adolescents ≥ 12 to < 18 years of age who are candidates for systemic therapy |
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| Company | Sanofi | ||
| BNF chapter | Skin | ||
| Assessment type | Limited | ||
| Status | Recommended with restrictions | ||
| Advice number | 1419 | ||
| NMG meeting date | 09/10/2019 | ||
| AWMSG meeting date | 13/11/2019 | ||
| Date of issue | 28/11/2019 | ||
| Commercial arrangement | PAS | ||