EMA recommends approval for ranibizumab biosimilar Rexatilux

Biosimilars/News | Posted 25/05/2026 post-comment0 Post your comment

On 23 April 2026, the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) adopted positive opinions, recommending the granting of a marketing authorization for Intas’ ranibizumab biosimilar, Rexatilux, for the treatment of wet macular degeneration.

Age-related macular degeneration V15b19

Ranibizumab is a monoclonal antibody fragment created from the same parent mouse antibody as bevacizumab. Ranibizumab inhibits angiogenesis (the formation of new blood vessels) by inhibiting vascular endothelial growth factor A (VEGF-A), a mechanism similar to bevacizumab [1]. 

Ranibizumab can be used to treat macular degeneration by inhibiting VEGF, which is responsible for the excessive formation of blood vessels in the retina leading to progressive loss of vision. The monoclonal antibody drug is indicated for the treatment of wet age-related macular degeneration (AMD), macular oedema, degenerative myopia and diabetes complications; all conditions of the eye causing vision loss [2].

Intas Third Party Sales 2005 SL’s Rexatilux is a biosimilar of Roche/Genentech’s Lucentis (ranibizumab). Rexatilux will be available as a 10 mg/mL solution for injection, and must be administered by a qualified ophthalmologist experienced in intravitreal injections.

Approved indications of Rexatilux:

  • neovascular (wet) age-related macular degeneration (AMD)
  • visual impairment due to diabetic macular oedema (DME)
  • proliferative diabetic retinopathy (PDR)
  • macular oedema secondary to retinal vein occlusion (branch RVO or central RVO)
  • choroidal neovascularisation (CNV).

The CHMP’s positive opinion was based on data demonstrating it is a biosimilar to the reference product, Lucentis. The EMA granted approval based on analytical, pharmacokinetic, and phase 3 clinical trial data proving it has comparable quality, safety, and efficacy to Lucentis.

Currently, six ranibizumab biosimilars are approved in Europe. The latest is Lupin’s Ranluspec [3]; others include Qilu Pharma’s Rimmyrah and Midas Pharma’s Epruvy (both approved in 2024), Bioeq/Teva’s Ranivisio and Stada’s Ximluci (both approved in 2022), and Samsung Bioepis’s Byooviz (approved in 2021).

There were no biosimilars approved in January and March 2026.

Related article
FDA approves third interchangeable ranibizumab biosimilar Nufymco

LATIN AMERICAN FORUM
The objective of GaBI’s Latin American Forum is to provide you with all the latest news and updates on developments of generic and biosimilar medicines in Latin America in Spanish.

View the latest headline article: Farmacopea Europea publica la primera monografía sobre un producto individual de anticuerpos monoclonales

Browse the news in the Latin American Forum!

Register to receive the GaBI Latin American Forum newsletter. Inform colleagues and friends of this new initiative.

FORO LATINOAMERICANO
El objetivo del Foro Latinoamericano de GaBI es brindarle las últimas noticias y actualizaciones sobre desarrollos de medicamentos genéricos y biosimilares en América Latina en español.

Ver el último artículo de cabecera: Farmacopea Europea publica la primera monografía sobre un producto individual de anticuerpos monoclonales

!Explore las noticias en el Foro Latinoamericano!

Regístrese para recibir el boletín informativo GaBI Foro Latinoamericano. Informe a colegas y amigos sobre esta nueva iniciativa. 

 

References
1. GaBI Online - Generics and Biosimilars Initiative. Biosimilars of bevacizumab [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2026 May 25]. Available from: www.gabionline.net/Biosimilars/General/Biosimilars-of-bevacizumab
2. GaBI Online - Generics and Biosimilars Initiative. Biosimilars of ranibizumab [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2026 May 25]. Available from: www.gabionline.net/biosimilars/general/Biosimilars-of-ranibizumab
3. GaBI Online - Generics and Biosimilars Initiative. EC approves golimumab biosimilar Gotenfia and ranibizumab biosimilar Ranluspec [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2026 May 25]. Available from: www.gabionline.net/biosimilars/news/ec-approves-golimumab-biosimilar-gotenfia-and-ranibizumab-biosimilar-ranluspec

Permission granted to reproduce for personal and non-commercial use only. All other reproduction, copy or reprinting of all or part of any ‘Content’ found on this website is strictly prohibited without the prior consent of the publisher. Contact the publisher to obtain permission before redistributing.

Copyright – Unless otherwise stated all contents of this website are © 2026 Pro Pharma Communications International. All Rights Reserved.

comment icon Comments (0)
Post your comment
Most viewed articles
About GaBI
Home/About GaBI Posted 05/08/2009
EU guidelines for biosimilars
EMA logo 1 V13C15
Home/Guidelines Posted 08/10/2010