EMA recommends approval of aflibercept biosimilars Afqlir and Opuviz

Biosimilars/News | Posted 23/10/2024 post-comment0 Post your comment

On 19 September 2024, the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) adopted a positive opinion, recommending the granting of marketing authorization for two aflibercept biosimilars:  Sandoz’s Afqlir and Samsung Bioepis’s Opuviz. These products are biosimilars of the reference product Eylea, developed by Regeneron and Bayer.

Age-related macular degeneration V15b19

Aflibercept is a vascular endothelial growth factor (VEGF) inhibitor [1], a recombinant fusion protein consisting of the extracellular domains of human VEGF receptor 1 and 2 fused to the Fc portion of human IgG1. By acting as a soluble decoy for the natural VEGF receptors, aflibercept inhibits their activation, thereby reducing angiogenesis.

Both Afqlir and Opuviz are approved for the treatment of: 

  • Neovascular (wet) age-related macular degeneration (AMD)
  • Macular oedema following retinal vein occlusion (branch RVO or central RVO)
  • Diabetic macular oedema (DME)
  • Myopic choroidal neovascularisation (myopic CNV)

The CHMP’s positive opinion of Opuviz was based on a totality of evidence including analytical, non-clinical data, and clinical data. A randomized, double-masked, parallel group, multicenter Phase 3 study demonstrated equivalent efficacy and comparable safety, immunogenicity, and pharmacokinetics (PK) profiles between SB15 and reference aflibercept (AFL). 

Both Afqlir and Opuviz are available as 40 mg/mL solution for injection in a vial. 

The first aflibercept biosimilar approved in Europe was Biocon’s Yesafili on 15 September 2023 [2].  With the approvals of two new aflibercept biosimilars, Afqlir and Opuviz, there are now three aflibercept biosimilars available in Europe.

Afqlir and Opuviz have already been approved by the FDA. Opuviz was approved as the first interchangeable biosimilar to Eylea in May 2024 [3]. Sandoz’s aflibercept biosimilar is called Afqlir in Europe and Enzeevu in the US [4]. Three other aflibercept biosimilars have been approved by the FDA: Yesafili (aflibercept-jbvf) [3], Ahzantive (aflibercept-mrbb) [5], and Pavblu (aflibercept-ayyh) [4]. This brings the total to five aflibercept biosimilars approved in the US to date.

Related article
International biosimilars players expanding their presence in China

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: Un innovador acuerdo de compra directa permite reducir drásticamente los precios de los biosimilares de adalimumab

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: Un innovador acuerdo de compra directa permite reducir drásticamente los precios de los biosimilares de adalimumab

!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 aflibercept [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2024 Oct 23]. Available from: www.gabionline.net/biosimilars/general/biosimilars-of-aflibercept
2. GaBI Online - Generics and Biosimilars Initiative. EC approval of natalizumab, aflibercept and tocilizumab biosimilars [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2024 Oct 23]. Available from: www.gabionline.net/biosimilars/news/ec-approval-of-natalizumab-aflibercept-and-tocilizumab-biosimilars
3. GaBI Online - Generics and Biosimilars Initiative. FDA approves first interchangeable aflibercept biosimilars to treat macular degeneration [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2024 Oct 23]. Available from: www.gabionline.net/biosimilars/news/fda-approves-first-interchangeable-aflibercept-biosimilars-to-treat-macular-degeneration
4. GaBI Online - Generics and Biosimilars Initiative. FDA approves aflibercept biosimilars Enzeevu and Pavblu [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2024 Oct 23]. Available from: www.gabionline.net/biosimilars/news/fda-approves-aflibercept-biosimilars-enzeevu-and-pavblu
5. GaBI Online - Generics and Biosimilars Initiative. FDA approves third aflibercept biosimilar Ahzantive [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2024 Oct 23]. Available from: www.gabionline.net/biosimilars/news/fda-approves-third-aflibercept-biosimilar-ahzantive

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 © 2024 Pro Pharma Communications International. All Rights Reserved.

comment icon Comments (0)
Post your comment
Related content
Canada approves pegfilgrastim biosimilar Armlupeg
Pegfilgrastim DrugBank V18K30
Biosimilars/News Posted 20/11/2024
FDA approves fifth ustekinumab biosimilar Imuldosa
11453696_l
Biosimilars/News Posted 13/11/2024
Most viewed articles
About GaBI
Home/About GaBI Posted 06/08/2009
EU guidelines for biosimilars
EMA logo 1 V13C15
Home/Guidelines Posted 08/10/2010