VABYSMO (faricimab) - Neovascular (wet) retrofoveal age-related macular degeneration (AMD)
Reason for request
New indication.
Key points
Favourable opinion for reimbursement “the treatment of neovascular (wet) retrofoveal age-related macular degeneration (AMD) in adults”.
What therapeutic improvement?
No clinical added value in the therapeutic strategy.
Role in the care pathway?
VABYSMO (faricimab) is a first-line treatment for neovascular (wet) retrofoveal age-related macular degeneration (AMD) in adults.
The choice between anti-VEGF therapies as first-line treatment is left to the decision of the ophthalmologist.
Special recommendations
The Committee recommends exception drug status.
Clinical Benefit
Substantial |
The clinical benefit of VABYSMO (faricimab) 120 mg/mL solution for injection is substantial in the treatment of neovascular (wet) retrofoveal age-related macular degeneration (AMD) in adults. |
Insufficient |
The clinical benefit of VABYSMO (faricimab) 120 mg/mL solution for injection is insufficient in other cases to justify public funding in view of the available alternatives. |
Clinical Added Value
no clinical added value |
Considering:
the Committee deems that VABYSMO (faricimab) solution for injection provides no clinical added value (CAV V) compared to EYLEA (aflibercept) solution for injection in pre-filled syringe in the treatment of neovascular (wet) retrofoveal age-related macular degeneration (AMD) in adults. |