AFQLIR (Sandoz Pty Ltd)
Product name
AFQLIR
Sponsor
Date registered
Evaluation commenced
Decision date
Approval time
200 (255 working days)
Active ingredients
Aflibercept
Registration type
New biosimilar medicine
Indication
[TRADE NAME] (aflibercept) 2 mg is indicated in adults for the treatment of:
- neovascular (wet) age-related macular degeneration (wet AMD)
- visual impairment due to macular oedema secondary to central retinal vein occlusion (CRVO)
- visual impairment due to macular oedema secondary to branch retinal vein occlusion (BRVO)
- diabetic macular oedema (DME)
- visual impairment due to myopic choroidal neovascularisation (myopic CNV).