FDA approves adalimumab biosimilar Cyltezo as interchangeable

Biosimilars/News | Posted 29/10/2021 post-comment0 Post your comment

The US Food and Drug Administration (FDA) has approved the first interchangeable adalimumab biosimilar. This is the second interchangeable biosimilar to gain FDA approval in the US and follows the landmark decision to approve an interchangeable insulin glargine biosimilar in July 2021 [1].

Switching mAb Pfizer V18K30

The agency announced on 18 October 2021 that on 15 October 2021 it had approved the adalimumab biosimilar Cyltezo (adalimumab-adbm) as the first interchangeable biosimilar to the reference product Humira (adalimumab).

The biosimilar is made by Germany-based Boehringer Ingelheim Pharmaceuticals (Boehringer Ingelheim). The company received approval from FDA for Cyltezo (BI 695501) on 25 August 2021 for the same indications as the reference product (AbbVie’s Humira), including ankylosing spondylitis (an arthritis that affects the spine), Crohn’s disease, psoriasis, psoriatic arthritis, rheumatoid arthritis and ulcerative colitis [2].

This new ‘interchangeable’ status means that Cyltezo may now be substituted for the reference product (AbbVie’s Humira) without the intervention of the prescriber. The substitution may occur at the pharmacy, a practice commonly called ‘pharmacy-level substitution’—much like how generics are substituted for brand-name drugs, subject to state pharmacy laws, which vary by state [3].

Cyltezo was also approved in Europe back in November 2017 but was withdrawn by Boehringer Ingelheim in January 2019 [4] after the company decided to pull out of the European biosimilars market and focus on the US [5].

Cyltezo is the second interchangeable biosimilar approved by FDA and the first interchangeable monoclonal antibody approved in the US.

Acting FDA Commissioner, Dr Janet Woodcock, said that the agency continues to be steadfast in its ‘commitment to provide patients with alternative high-quality, affordable medications that are proven to be safe and effective’. She added that ‘the biosimilar and interchangeable approval pathway was created to help increase access to treatment options for patients with serious medical conditions.’

Related articles
Biosimilars approved in the US

Biosimilars of adalimumab

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 this week’s headline article: Los datos apoyan la intercambiabilidad de los biosimilares de 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.

LATIN AMERICAN FORUM

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.

Vea el artículo principal de esta semana: Los datos apoyan la intercambiabilidad de los biosimilares de 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. FDA approves first interchangeable insulin glargine biosimilar [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2021 Oct 29]. Available from: www.gabionline.net/biosimilars/news/fda-approves-first-interchangeable-insulin-glargine-biosimilar
2. GaBI Online - Generics and Biosimilars Initiative. FDA approves adalimumab biosimilar Cyltezo [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2021 Oct 29]. Available from: www.gabionline.net/biosimilars/news/FDA-approves-adalimumab-biosimilar-Cyltezo
3. GaBI Online - Generics and Biosimilars Initiative. 45 US states have passed biosimilar substitution laws [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2021 Oct 29]. Available from: www.gabionline.net/policies-legislation/45-US-states-have-passed-biosimilar-substitution-laws
4. GaBI Online - Generics and Biosimilars Initiative. Biosimilars approved in Europe [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2021 Oct 29]. Available from: www.gabionline.net/biosimilars/general/biosimilars-approved-in-Europe
5. GaBI Online - Generics and Biosimilars Initiative. Boehringer Ingelheim and Sandoz abandon biosimilars [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2021 Oct 29]. Available from: www.gabionline.net/biosimilares/general/Boehringer-Ingelheim-and-Sandoz-abandon-biosimilars

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 © 2021 Pro Pharma Communications International. All Rights Reserved.

Source: EMA, US FDA

comment icon Comments (0)
Post your comment
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