On 25 April 2024, the European Medicine Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) adopted positive opinions for two biosimilar medicines: Tofidence (tocilizumab) and Wezenla (ustekinumab), recommending the granting of marketing authorization. This comes following news that Wezlana reached the market in Canada in early March 2024.
EMA recommends approval of biosimilar tocilizumab Tofidence and ustekinumab Wezenla
Biosimilars/News | Posted 05/06/2024 0 Post your comment
Tofidence (tocilizumab)
Tofidence (tocilizumab) is a biosimilar of Roche’s Actemra (tocilizumab). Tofidence was developed as a result of a partnership between Biogen and Bio-Thera Solutions [1] and is approved for the treatment of rheumatoid arthritis (RA), systemic juvenile idiopathic arthritis (sJIA), polyarticular juvenile idiopathic arthritis (pJIA), and coronavirus disease 2019 (COVID-19).
Tocilizumab is a humanized monoclonal antibody which acts against the interleukin-6 receptor (IL-6R). It is an immunosuppressive drug used mainly for the treatment of rheumatoid arthritis and polyarticular juvenile idiopathic arthritis, and systemic juvenile idiopathic arthritis [2].
Tofidence has received EMA approval for both subcutaneous and intravenous formulations. It will be available as a 20 mg/mL concentrate for solution for infusion.
Tofidence (tocilizumab-bavi) is the first tocilizumab biosimilar to gain approval in the US, which was granted in September 2023 [3].
Tofidence will become the second tocilizumab biosimilar available in Europe, following Fresenius Kabi’s Tyenne, which received EC approval on 15 September 2023 [4].
Wezenla (ustekinumab)
Wezenla (ustekinumab) is a biosimilar to Johnson & Johnson’s Stelara (ustekinumab). Wezenla was developed by Amgen and is approved for the treatment of plaque psoriasis, including paediatric plaque psoriasis, psoriatic arthritis and Crohn’s disease.
Ustekinumab is a humanized monoclonal antibody that interferes with the triggering of the body’s inflammatory response through the suppression of certain cytokines. Specifically, it blocks interleukin IL 12 and IL 23 which help activate certain T cells. It binds to the p 40 subunit of both IL 12 and IL 23 so that they subsequently cannot bind to their receptors. It is indicated for the treatment of Crohn’s disease, psoriasis and psoriatic arthritis [5].
Wezenla will be available as 45 mg and 90 mg solution for injection and 130 mg concentrate for solution for infusion.
Amgen’s biosimilar ustekinumab is called Wezenla in Europe and Wezlana in Canada [6] and the US [7].
Wezlana was the first approved biosimilar of Stelara in the US, where it has the interchangeability designation [7]. It is also one of the first 10 drugs to be selected as part of Medicare Drug Price Negotiation Program, which seeks to reduce biosimilars prices as part of the Inflation Reduction act [8].
Related article
EMA recommends approval of ustekinumab biosimilar Pyzchiva
LATIN AMERICAN FORUM View the latest headline article: Guía de la FDA sobre etiquetado promocional y publicidad de productos biológicos, biosimilares e intercambiables 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 Ver el último artículo de cabecera: Guía de la FDA sobre etiquetado promocional y publicidad de productos biológicos, biosimilares e intercambiables !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. FDA approves first tocilizumab biosimilar Tofidence [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2024 Jun 5]. Available from: www.gabionline.net/biosimilars/news/fda-approves-first-tocilizumab-biosimilar-tofidence
2. GaBI Online - Generics and Biosimilars Initiative. Biosimilars of tocilizumab [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2024 Jun 5]. Available from: www.gabionline.net/biosimilars/general/Biosimilars-of-tocilizumab
3. 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 Jun 5]. Available from: www.gabionline.net/biosimilars/news/ec-approval-of-natalizumab-aflibercept-and-tocilizumab-biosimilars
4. 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 Jun 5]. Available from: www.gabionline.net/biosimilars/news/ec-approval-of-natalizumab-aflibercept-and-tocilizumab-biosimilars
5. GaBI Online - Generics and Biosimilars Initiative. Biosimilars of ustekinumab [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2024 Jun 5]. Available from: www.gabionline.net/biosimilars/general/biosimilars-of-ustekinumab
6. GaBI Online - Generics and Biosimilars Initiative. Three more biosimilar approvals in Canada in 2023 [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2024 Jun 5]. Available from: www.gabionline.net/biosimilars/news/three-more-biosimilar-approvals-in-canada-in-2023
7. GaBI Online - Generics and Biosimilars Initiative. FDA approves first interchangeable ustekinumab biosimilar Wezlana [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2024 Jun 5]. Available from: www.gabionline.net/biosimilars/news/fda-approves-first-interchangeable-ustekinumab-biosimilar-wezlana
8. GaBI Online - Generics and Biosimilars Initiative. Four drugmakers sue the US government over the Inflation Reduction Act [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2024 Jun 5]. Available from: www.gabionline.net/pharma-news/four-drugmakers-sue-the-us-government-over-the-inflation-reduction-act
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.
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
Biosimilar medicines on the Pharmaceutical Benefits Scheme in Australia
SBR issues consensus on interchangeability of reference products and biosimilars
Comments (0)
Post your comment