Following a full submission:
perampanel (Fycompa®) is accepted for restricted use within NHS Scotland.
Indication under review: Adjunctive treatment of partial-onset seizures with or without secondarily generalised seizures in patients with epilepsy aged 12 years and older.
SMC restriction: use as a second-line adjunctive treatment in patients with refractory partial onset epilepsy. Treatment should be initiated only by physicians who have appropriate experience in the treatment of epilepsy.
In three placebo-controlled studies in patients with uncontrolled partial-onset seizures, perampanel was superior to placebo in terms of the proportion of patients experiencing a ≥50% reduction in partial seizure frequency per 28 days.
This SMC advice takes account of the benefits of a Patient Access Scheme (PAS) that improves the cost-effectiveness of perampanel. This SMC advice is contingent upon the continuing availability of the patient access scheme or a list price that is equivalent or lower.
Download detailed advice153KB (PDF)
Medicine details
- Medicine name:
- perampanel (Fycompa)
- SMC ID:
- 819/12
- Indication:
- As adjunctive treatment for partial-onset seizures with or without secondarily generalized seizures in patients with epilepsy aged 12 years and older.
- Pharmaceutical company
- Eisai Ltd
- BNF chapter
- Central nervous system
- Submission type
- Full
- Status
- Restricted
- Date advice published
- 10 December 2012