<p>Vgenfli is a medicine used to treat adults with:</p><ul><li>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 and cause swelling;</li><li>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);</li><li>impaired vision due to macular oedema caused by diabetes;</li><li>impaired vision due to choroidal neovascularisation in people with myopia (short-sightedness).</li></ul><p>Vgenfli contains the active substance aflibercept and is a biological medicine. It is a ‘biosimilar medicine’; this means that Vgenfli is highly similar to another biological medicine (the ‘reference medicine’) that is already authorised in the EU. The reference medicine for Vgenfli is Eylea. For more information on biosimilar medicines, see <a href="https://www.ema.europa.eu/en/human-regulatory/overview/biosimilar-medicines">here</a>.</p>
Therapeutic Indication
<div class="subsection mt-3-5"> <h3>Therapeutic indication</h3><p>Vgenfli is indicated for adults for the treatment of<br>- neovascular (wet) age-related macular degeneration (AMD),<br>- visual impairment due to macular oedema secondary to retinal vein occlusion (branch RVO or central RVO),<br>- visual impairment due to diabetic macular oedema (DME),<br>- visual impairment due to myopic choroidal neovascularisation (myopic CNV).</p></div>
Therapeutic Area (MeSH)
ATC Code
S01LA05
ATC Item
N/A
Pharmacotherapeutic Group
Ophthalmologicals
Active Substance (Summary)
INN / Common Names
| Substance | CAS | Monograph |
|---|---|---|
| aflibercept | N/A | aflibercept |
EMA Name
Vgenfli
Medicine Name
Vgenfli
Aliases
N/ANo risk management plan link.