- Indication
- Choroidal neovascularisation (CNV) associated with pathological myopia
- RAG rating
- Red
- Document type
- Decision document
- Place
- Hertfordshire and West Essex ICB
- Output type
- Pharmacy / Prescribing
Ranibizumab
HERTFORDSHIRE AND WEST ESSEX AREA PRESCRIBING COMMITTEE (HWE APC)
Aflibercept 2mg biosimilar
and Ranibizumab biosimilar for Choroidal neovascularisation (CNV)
RED
Recommended for restricted prescribing by specialist only.
Not recommended for primary care prescribing.
Name generic (trade) Aflibercept 2mg biosimilar and Ranibizumab biosimilar
What it is Vascular endothelial growth factor A inhibitor (anti-VEGF)
Indication Choroidal neovascularisation (CNV) associated with pathological myopia
Date decision last revised January 2026
Decision status Final
NICE / SMC Guidance NICE TA 486 and NICE TA 298 recommended.
HWE APC recommendation:
Treatment options consistent with NICE TA
recommendations for approved indications:
- ranibizumab
biosimilar and aflibercept 2mg biosimilar are the preferred first line
anti-VEGF agents
- aflibercept
2mg biosimilar is
the preferred second line anti-VEGF agent if 1st line ranibizumab
biosimilar used
- clinicians
should consider reviewing patients currently prescribed ranibizumab
(Lucentis®) and aflibercept (Eylea) to assess suitability for a change to
biosimilars
Review date: The recommendation is based upon the
evidence available at the time of publication. This recommendation will be
reviewed upon request in the light of new evidence becoming available.
Updated August 2025 to reflect
availability of aflibercept 2mg biosimilar Q3 2025 and updated wet AMD
prescribing guideline, approved July 2025 APC. Updated January 2026 to reflect
the diabetic macular oedema guideline and macular oedema secondary to retinal
vein occlusion guideline, approved December 2025 APC.