following a full submission:
adalimumab 40mg solution for injection (Humira) is accepted for restricted use within NHS Scotland for treatment of chronic plaque psoriasis in adult patients who failed to respond to or have a contraindication to or are intolerant to other systemic therapy including ciclosporin methotrexate or PUVA.
Its use should be restricted to patients with severe disease as defined by a total Psoriasis Area Severity Index (PASI) score of ≥10 and a Dermatology Life Quality Index (DLQI) of >10. Adalimumab improves both signs and symptoms of psoriasis and quality of life compared to placebo and an active non-biological comparator. The manufacturer presented a sufficiently robust economic case to gain acceptance by the SMC for patients with severe disease who achieve a PASI 75 response from baseline at 16 weeks. Continuation of therapy beyond 16 weeks should be carefully reconsidered in patients not responding within this time period.
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Medicine details
- Medicine name:
- adalimumab (Humira)
- SMC ID:
- 468/08
- Indication:
- Moderate to severe chronic plaque psoriasis in adult patients
- Pharmaceutical company
- Abbott Laboratories
- BNF chapter
- Skin
- Submission type
- Full
- Status
- Restricted
- Date advice published
- 09 June 2008