STADA and Xbrane obtain British approval for Ximluci (ranibizumab) biosimilar referencing Lucentis

The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) has granted a marketing authorization for STADA and Xbrane’s Ximluci (ranibizumab), a biosimilar referencing Lucentis. STADA is preparing to launch Ximluci in the UK during 2023.

Xbrane’s contribution to the partnership includes a patented protein-expression system and Europe-based production set-up, while STADA brings considerable heritage supplying biosimilars and other specialty medicines in the UK.

“Considerable unmet need for biologic ophthalmic treatments exists in the UK and throughout Europe,” said Bryan Kim, STADA’s head of Specialty Care. “With almost 15 years’ experience of supplying biosimilars, STADA looks forward to working with Xbrane, as well as with NHS and our commercial partners, to broaden patient access to ranibizumab and optimize use of healthcare resources in the UK.”

“We are proud to have worked with STADA to take this molecule, developed under the XlucaneTM name, from cell-line development to approval and manufacturing, based on our patented expression system, in Europe,” stated Martin Åmark, CEO of Xbrane.

Ximluci is an anti-VEGF (vascular endothelial growth factor) for the treatment of retinal vascular disorders, which are a leading cause of blindness globally. Ximluci has been approved in the UK for treating wet age-related macular degeneration (wet AMD), diabetic macular oedema (DME), diabetic retinopathy (PDR), retinal vein occlusion (RVO) and visual impairment due to choroidal neovascularization (CNV) in adults.

According to the UK’s Macular Society, nearly 1.5 million people in the UK have macular disease. Age-related macular degeneration is the most common condition, generally affected people aged over 55. AMD is the biggest cause of sight loss in the UK, affecting more than 600,000 people.

The British marketing authorization was granted via the EC Decision Reliance Procedure (ECDRP), whereby the MHRA relied on the decision taken by the European Commission (EC) on 9 November 2022 to issue a centralized marketing authorization for Ximluci valid in all 27 European Union member states, as well as in Iceland, Norway and Liechtenstein. The European Medicines Agency had determined Ximluci to be highly similar to the reference product, Lucentis, based on data showing comparable quality, safety and efficacy to Lucentis.

The British marketing authorization for Ximluci 10 mg/ml solution for injection is held by STADA’s Genus Pharmaceuticals subsidiary.

In July 2018, STADA and Xbrane entered into an agreement under which the two companies are jointly responsible for development and for manufacturing the finished product. STADA holds the marketing authorizations and the commercial rights to the biosimilar across all territories included in the agreement, which covers Europe, the US, several countries in the Middle East and North Africa (MENA) region, and selected Asia-Pacific (APAC) markets.

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