European CHMP recommends approval of ranibizumab (Byooviz) for treatment of various ocular conditions

Byooviz is a biosimilar that has comparable quality, safety and efficacy to Lucentis (ranibizumab). It is available as a 10 mg/ml solution for injection as will be licensed for similar indications to Lucentis.

SPS commentary:

It is unclear when a biosimilar version of ranibizumab will become available as the patent for Lucentis is likely to be in place until 2022.

Source:

European Medicines Agency