Yesafili is a medicine used to treat adults with: - the ‘wet’ form of age-related macular degeneration (AMD), a disease which affects the central part of the retina (called the macula) at the back of the eye. The wet form of AMD is caused by choroidal neovascularisation (the abnormal growth of blood vessels under the macula), which may leak fluid and blood, causing swelling; - impaired vision due to macular oedema (swelling) that follows blockage of either the main vein carrying blood from the retina (known as central retinal vein occlusion, CRVO) or of smaller branch veins (known as branch retinal vein occlusion, BRVO); - impaired vision due to macular oedema caused by diabetes; - impaired vision due to myopic choroidal neovascularisation (a severe type of short-sightedness where the eyeball continues to grow, becoming longer than it should be). Yesafili is a ‘biosimilar medicine’. This means that Yesafili is highly similar to another biological medicine (the ‘reference medicine’) that is already authorised in the EU. The reference medicine for Yesafili is Eylea. For more information on biosimilar medicines, see [here](/en/biosimilar-medicines-overview). Yesafili contains the active substance aflibercept.
Therapeutic Indication
### Therapeutic indication Yesafili is indicated for adults for the treatment of - neovascular (wet) age-related macular degeneration (AMD) (see section 5.1), - visual impairment due to macular oedema secondary to retinal vein occlusion (branch RVO or central RVO) (see section 5.1), - visual impairment due to diabetic macular oedema (DME) (see section 5.1), - visual impairment due to myopic choroidal neovascularisation (myopic CNV) (see section 5.1).
Therapeutic Area (MeSH)
ATC Code
S01LA05
ATC Item
aflibercept
Pharmacotherapeutic Group
Ophthalmologicals
Active Substance (Summary)
INN / Common Names
| Substance | CAS | Monograph |
|---|---|---|
| aflibercept | N/A | 阿柏西普 |
EMA Name
Yesafili
Medicine Name
Yesafili
Aliases
N/A