Ranluspec is a medicine used to treat adults with certain sight problems caused by damage to the retina (the light\-sensing layer at the back of the eye), and more specifically its central region, known as the macula. The macula provides the vision needed to see detail for everyday tasks such as driving, reading and recognising faces. In adults, Ranluspec is used to treat: * ‘wet’ form of age\-related macular degeneration (AMD). The wet form of AMD is caused by choroidal neovascularisation (abnormal growth of blood vessels beneath the retina, which may leak fluid and blood and cause swelling); * macular oedema (swelling of the macula) caused by diabetes or by occlusion (blockage) of the veins behind the retina; * proliferative diabetic retinopathy (growth of abnormal tiny blood vessels in the eye, associated with diabetes); * other sight problems associated with choroidal neovascularisation. Ranluspec contains the active substance ranibizumab and is a biological medicine. It is a ‘biosimilar medicine’; this means that Ranluspec is highly similar to another biological medicine (the ‘reference medicine’) that is already authorised in the EU. The reference medicine for Ranluspec is Lucentis. For more information on biosimilar medicines, see [here](https://www.ema.europa.eu/en/human-regulatory/overview/biosimilar-medicines).
Therapeutic Indication
Ranluspec is indicated in adults for: The treatment of neovascular (wet) age\-related macular degeneration (AMD) The treatment of visual impairment due to diabetic macular oedema (DME) The treatment of proliferative diabetic retinopathy (PDR) The treatment of visual impairment due to macular oedema secondary to retinal vein occlusion (branch RVO or central RVO) The treatment of visual impairment due to choroidal neovascularisation (CNV)
Therapeutic Area (MeSH)
ATC Code
S01LA04
ATC Item
N/A
Pharmacotherapeutic Group
Ophthalmologicals
Active Substance (Summary)
INN / Common Names
EMA Name
Ranluspec
Medicine Name
Ranluspec
Aliases
N/ANo risk management plan link.