Advice

following a full submission

aflibercept (Eylea®) is accepted for restricted use within NHS Scotland.

Indication under review: For adults for the treatment of visual impairment due to diabetic macular oedema (DMO).

SMC restriction: treatment of visual impairment due to DMO in adults with best corrected visual acuity (BCVA) 75 Early Treatment Diabetic Retinopathy Study (ETDRS) letters or less at baseline.

Intravitreal aflibercept significantly improved BCVA at 52 weeks compared with laser photocoagulation in two phase III, double-masked studies.

This advice takes account of the benefits of a Patient Access Scheme (PAS) that improves the cost-effectiveness of aflibercept. This advice is contingent upon the continuing availability of the patient access scheme, or a list price that is equivalent or lower, in NHS Scotland.

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Medicine details

Medicine name:
aflibercept (Eylea)
SMC ID:
1003/14
Indication:
Treatment of visual impairment due to DMO in adults with best corrected visual acuity (BCVA) 75 Early Treatment Diabetic Retinopathy Study (ETDRS) letters or less at baseline.
Pharmaceutical company
Bayer plc/Bayer Schering Pharma
BNF chapter
Eye
Submission type
Full
Status
Restricted
Date advice published
10 November 2014