AbbVie antitrust investigation and Sandoz biosimilar delay

INICIO/Noticias Farmacéuticas | Posted 04/06/2021 post-comment0 Post your comment

In May 2021, following the release of a report, it was announced that AbbVie is likely to be subject to an antitrust investigation due to claims it has delayed market entry of biosimilars of Humira (adalimumab). Alvotech also raised a complaint against AbbVie after being sued over their Humira biosimilar application. In addition, the US Supreme Court denied Sandoz the ability to release its Enbrel (etanercept) biosimilar.

Antitrust V21F04

AbbVie antitrust investigation
In the US, it has been requested that the Federal Trade Commission (FTC) opens an antitrust investigation into pharmaceutical company AbbVie. The company has allegedly taken action to prevent competition for its inflammatory disease drug Humira.

This announcement came after the release of a report from the House Committee on Oversight and Reform that outlines attempts by AbbVie to prevent biosimilar versions of Humira entering the market. Although six biosimilar versions of the product have been approved by the US Food and Drug Administration (FDA), and some could have entered the market by 2017, these have been held back until 2023 due to AbbVie’s litigation and negotiated settlements. The maintenance of the AbbVie monopoly has allowed the company to reap huge profits in the US, including US$16 billion net revenue for Humira in 2020 alone.

Alvotech vs AbbVie
This request follows the complaint filed by Alvotech USA and Alvotech ehf (jointly, Alvotech) against AbbVie Inc and AbbVie Biotechnology Ltd (jointly, AbbVie) in the Eastern District of Virginia in early May 2021. Alvotech is seeking declaratory judgment as it alleges that it was incorrectly sued by AbbVie over a Humira biosimilar application, as Alvotech ehf rather than Alvotech USA.

Delayed market entry for Sandoz’s etanercept biosimilar
Also in May 2021, it was announced that the US Supreme Court denied a petition by pharmaceutical company, Sandoz, to review the decision concerning its biosimilar of Amgen’s Enbrel (etanercept), named Erelzi (etanercept-szzs).

This decision means that Sandoz’s more affordable Erelzi, which was approved for use in the US in 2016, will not be available in the US to treat patients with autoimmune and inflammatory diseases until 2029.

Related articles
EMA and FDA accept application for adalimumab biosimilar AVT02

Court rules Amgen’s patents on Enbrel are valid, Sandoz to appeal

LATIN AMERICAN FORUM – Coming soon!

To further enhance the objectives of GaBI in sharing information and knowledge that ensure policies supportive of safe biosimilars use, we are pleased to announce that we will be launching a new section on GaBI Online and GaBI Journal, the ‘Latin American Forum’ (in Spanish) featuring the latest news and updates on research and developments in generic and biosimilar medicines in Latin America.

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

 

LATIN AMERICAN FORUM – Próximamente!

Para fomentar los objetivos de GaBI sobre la difusión de información y conocimiento sobre las políticas de apoyo que garantizan el uso seguro de medicamentos biosimilares, nos complace anunciar el lanzamiento de una nueva sección en GaBI Online y GaBI Journal, el ‘Latin American Forum’ (en español), que presentará las últimas noticias y actualizaciones en investigación y desarrollo sobre medicamentos genéricos y biosimilares en Latinoamérica.

Regístrese para recibir el boletín informativo GaBI Latin American Forum. Informe a colegas y amigos sobre esta nueva iniciativa. 

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.

comment icon Comments (0)
Post your comment
Related content
Licensing agreements signed for ustekinumab biosimilars
IBD 1
INICIO/Noticias Farmacéuticas Posted 17/09/2021
Oncogen–BrightGene partnership
104 MD001918
INICIO/Noticias Farmacéuticas Posted 10/09/2021
Menagen–CKD Middle Eastern partnership
01 AA007239
INICIO/Noticias Farmacéuticas Posted 03/09/2021
Teva signs deal with Bioeq for ranibizumab biosimilar FYB201
VEGF allaboutvision.com V21D02
INICIO/Noticias Farmacéuticas Posted 30/07/2021
Most viewed articles
Sobre GaBI
INICIO/Sobre GaBI Posted 05/08/2009
EU guidelines for biosimilars
EMA logo 1 V13C15
INICIO/Directrices Posted 08/10/2010