Following a limited submission
AWMSG advice |
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Status: Recommended with restrictions | |||
Belimumab (Benlysta®) is recommended as an option for restricted use within NHS Wales. Belimumab (Benlysta®) is licensed as add-on therapy in patients aged 5 years to < 18 years old with active, autoantibody-positive systemic lupus erythematosus with a high degree of disease activity (e.g. positive anti-dsDNA and low complement) despite standard therapy. Belimumab (Benlysta®) is restricted for the treatment of patients who have serological disease activity (defined as positive anti-double-stranded DNA and low complement) and a Safety of Estrogen in Lupus National Assessment – Systemic Lupus Erythematosus Disease Activity Index (SELENA-SLEDAI) score greater than or equal to 10 despite standard treatment. Belimumab (Benlysta®) treatment should be continued beyond 24 weeks only if the SELENA-SLEDAI score has improved by 4 points or more. Belimumab (Benlysta® ) 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/WPAS price. |
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Medicine details |
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Medicine name | belimumab (Benlysta®) | ||
Formulation | 120 mg powder for concentrate for solution for infusion, 400 mg powder for concentrate for solution for infusion | ||
Reference number | 3778 | ||
Indication | Treatment of systemic lupus erythematosus in children |
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Company | GlaxoSmithKline | ||
BNF chapter | Immunological products & vaccines | ||
Submission type | Limited | ||
Status | Recommended with restrictions | ||
Advice number | 0720 | ||
NMG meeting date | 25/06/2020 | ||
AWMSG meeting date | 15/07/2020 | ||
Date of issue | 04/08/2020 | ||
Commercial arrangement | PAS |