DUBLIN, Dec. 14, 2023 /PRNewswire/ -- The "Adalimumab (Humira) Biosimilars Pipeline Review" report has been added to ResearchAndMarkets.com's offering.
This product provides basic information on approved drugs and drug candidates in research and development as biosimilar antibodies of Humira (adalimumab). In January 2013, Abbott completed the separation of its research-based pharmaceuticals business, which became AbbVie, a new independent biopharmaceutical company. Humira generated cumulative worldwide (ex Japan) sales for Abbott/AbbVie of more than US$ 213 bln. Eisai holds commercialization rights for Humira in Japan. Adalimumab is a recombinant human IgG1 monoclonal antibody created using phage display technology resulting in an antibody with human derived heavy and light chain variable regions and human IgG1:k constant regions. Adalimumab is produced by recombinant DNA technology in a mammalian cell (Chinese Hamster Ovary (CHO)) expression system and is purified by a process that includes specific viral inactivation and removal steps. It consists of 1330 amino acids and has a molecular weight of approximately 148 kilodaltons. Humira's main patents expired in 2016 and first biosimilar versions of Humira were launched in Europe in 2018. AbbVie filed about 250 patent applications for Humira in the U.S., 90% of them following the drug's 2002 approval. The strengthened patent shield has stretched AbbVie's legal monopoly in the U.S. for six years beyond the expiration of Humira's main patent in 2016. Amgen was the first to launch its Humira biosimilar in the US in January 2023, and more entries of Humira biosimilars into the US market are scheduled over the course of 2023, mainly in July. Biosimilars are follow-on versions of biopharmaceuticals, for which exclusivity has expired. They are approved via stringent regulatory pathways in highly regulated markets (such as EU, US, Japan, Canada, Australia) based on proven similarity of the biosimilar with the originator biopharmaceutical reference product.
In the US, Humira is approved for treatment of Non-infectious intermediate, posterior, and panuveitis in adults and children 2 years of age and older.
This product consists of:
Competitors described in a tabular format covering drug code/INN, target(s)/MoA, class of compound, territory of main competitor, indication(s) & R&D stage, including published sales data.
Project History with link to source of information (press release, homepage, abstracts, presentations, annual reports etc).
One-month online access to the publisher's database for adalimumab biosimilars (prerequisite: access to internet). For more information about this report visit https://www.researchandmarkets.com/r/yqjxx7
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