Fresenius Kabi and Formycon receive US FDA approval for biosimilar Otulfi (ustekinumab-aauz)

30 September 2024 - In accordance with the patent settlement between Fresenius Kabi, Formycon and Johnson & Johnson, Fresenius Kabi has ...

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Sandoz receives FDA approval for Enzeevu (aflibercept-abzv), further strengthening US biosimilar position

12 August 2024 - Enzeevu (aflibercept-abzv) approved to treat neovascular age-related macular degeneration. ...

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Bio-Thera Solutions announces regulatory filing acceptance for BAT2206, a proposed biosimilar to Stelara in the US and EU

24 July 2024 - The BAT2206 BLA and MAA are based on a robust analytical, non-clinical and clinical data package ...

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FDA approves Samsung Bioepis’ Epysqli (eculizumab-aagh) as a biosimilar to Soliris (eculizumab)

22 July 2024 - Epysqli is approved for the treatment of patients with paroxysmal nocturnal haemoglobinuria and atypical haemolytic uremic syndrome. ...

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Boehringer Ingelheim and GoodRx announce exclusive patient affordability initiative for adalimumab-adbm injection, Boehringer’s biosimilar to Humira

18 July 2024 - First biosimilar with an exclusive low cash price on the GoodRx platform. ...

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FDA grants approval for Eylea biosimilar FYB203/Azhantive (aflibercept-mrbb)

28 June 2024 - Formycon and its licensing partner Klinge Biopharma announce that the US FDA today approved FYB203/Azhantive (aflibercept-mrbb), ...

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FDA approves biosimilar Pyzchiva (ustekinumab-ttwe), to be commercialised by Sandoz in US

1 July 2024 - FDA granted provisional determination for interchangeability designation for Pyzchiva. ...

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FDA approves first interchangeable biosimilar for two rare diseases

28 May 2024 - Today, the US FDA approved Bkemv (eculizumab-aeeb) as the first interchangeable biosimilar to Soliris (eculizumab) to ...

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Fresenius announces FDA acceptance for review of denosumab biosimilar application

27 May 2024 - Fresenius announced today that the US FDA has accepted for review the company’s biologics license application ...

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Teva and Alvotech announce Simlandi (adalimumab-ryvk) injection now available in the US

20 May 2024 - Simlandi is the first interchangeable high concentration, citrate-free biosimilar to Humira. ...

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FDA approves first interchangeable biosimilars to Eylea to treat macular degeneration and other eye conditions

20 May 2024 - Today, FDA approved Yesafili (aflibercept-jbvf) and Opuviz (aflibercecpt-yszy) as the first interchangeable biosimilars to Eylea (aflibercept). ...

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Boehringer Ingelheim expands access to adalimumab-adbm injection, the company's biosimilar to Humira

13 May 2024 - Boehringer Ingelheim announced an agreement with Quallent Pharmaceuticals, a private label pharmaceutical distributor, to help expand patient ...

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Celltrion USA's adalimumab-aaty biosimilar to Humira now available at low wholesale acquisition cost

9 May 2024 - Adalimumab-aaty will be priced at an 85% discount to Humira (adalimumab). ...

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US FDA approves high concentration, citrate-free formulation of Cyltezo (adalimumab-adbm) injection, Boehringer Ingelheim's interchangeable biosimilar to Humira

1 May 2024 - Boehringer Ingelheim announced today that the US FDA has approved the high concentration, citrate-free formulation of ...

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A milestone in facilitating the development of safe and effective biosimilars

26 April 2024 - This week, the FDA approved the 50th biosimilar, reflecting the markedly increased availability of biosimilar products—products that ...

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