On 18 August 2022, South Korea-based biologicals specialist Celltrion announced that its bevacizumab biosimilar, Vegzelma (CT-P16), had received European Commission (EC) approval.
EC approves bevacizumab biosimilar Vegzelma
Biosimilars/News | Posted 23/09/2022 0 Post your comment
Bevacizumab is a humanized monoclonal antibody. It inhibits angiogenesis (the formation of new blood vessels) by blocking the action of vascular endothelial growth factor A (VEGF-A). Bevacizumab can therefore slow the growth of new blood vessels in tumours and is used to treat various cancers, including colorectal, lung, breast, glioblastoma, kidney and ovarian. The originator product, Avastin, is sold by Roche/Genentech [1].
The European Commission (EC) has approved Vegzelma for the treatment of metastatic breast cancer, non-small cell lung cancer, advanced and/or metastatic renal cell cancer, metastatic carcinoma of the colon or rectum, ovarian cancer and cervical cancer.
The EC approval follows a positive opinion issued in June 2022 by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) and is applicable to all 27 European Union Member States plus Iceland, Norway and Liechtenstein [2].
The positive CHMP opinion was supported by a comprehensive data package, including a phase III clinical trial in patients with metastatic or recurrent non-squamous non-small cell lung cancer, and the totality of evidence demonstrates biosimilarity to Avastin for all indications.
This bevacizumab biosimilar is Celltrion’s third oncology biosimilar approved by the EC. The company has also applied for marketing approval for this bevacizumab biosimilar (CT-P16) in Korea and the US [3].
Related articles
Innovent-Etana bevacizumab biosimilar approved in Indonesia
FDA approves Amneal’s bevacizumab biosimilar
EC and FDA approval for first ranibizumab biosimilar Byooviz
EC approval for bevacizumab biosimilar Alymsys/Oyavas
LATIN AMERICAN FORUM The new section of the ‘Latin American Forum’ on GaBI has been launched. The objective of this new section 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: La EMA pide la intercambiabilidad de los biosimilares en toda la UE 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 Se ha lanzado la nueva sección del ‘Foro Latinoamericano’ sobre GaBI. El objetivo de esta nueva sección 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: La EMA pide la intercambiabilidad de los biosimilares en toda la UE !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 2022 Sep 23]. Available from: www.gabionline.net/biosimilars/general/Biosimilars-of-bevacizumab
2. GaBI Online - Generics and Biosimilars Initiative. EMA recommends approval of bevacizumab biosimilar vegzelma [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2022 Sep 23]. Available from: www.gabionline.net/biosimilars/news/ema-recommends-approval-of-bevacizumab-biosimilar-vegzelma
3. GaBI Online - Generics and Biosimilars Initiative. Celltrion seeks approval for bevacizumab biosimilar in Europe, US and Korea [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2022 Sep 23]. Available from: www.gabionline.net/biosimilars/news/celltrion-seeks-approval-for-bevacizumab-biosimilar-in-europe-us-and-korea
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 © 2022 Pro Pharma Communications International. All Rights Reserved.
Research
Long-term real-world safety experience of biosimilars confirms concept of biosimilarity
Budget impact analysis of Rixathon introduction in Chile for non-Hodgkin lymphoma
General
SBR issues consensus on interchangeability of reference products and biosimilars
Innovative direct purchase agreement sees adalimumab biosimilar prices slashed
Comments (0)
Post your comment