Alvotech provides update on status of US biologics license application for AVT04

12 October 2023 - Alvotech announced today that the US FDA has issued a complete response letter for Alvotech’s biologics ...

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Biocon biologics receives complete response letter from US FDA for biosimilar insulin aspart

7 October 2023 - The US FDA has issued a complete response letter for the biologics license application for insulin aspart.  ...

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FDA grants interchangeable designation to Pfizer’s biosimilar Abrilada

5 October 2023 - Interchangeable designation supported by positive data from the REFLECTIONS B538-12 study. ...

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Coherus announces resubmission of biologics license application supplement for Udenyca Onbody

5 October 2023 - Resubmission follows the satisfactory resolution of the FDA’s review of inspection findings at the third-party filler. ...

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Adalimumab-adbm, Boehringer Ingelheim’s Interchangeable biosimilar to Humira, now available at low wholesale acquisition cost

2 October 2023 - Adalimumab-adbm will be priced at an 81% discount to Humira (adalimumab). ...

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Formycon and Fresenius Kabi announce EMA acceptance of the marketing authorisation application for FYB202, an ustekinumab biosimilar candidate

29 September 2023 - Formycon and its commercialisation partner Fresenius Kabi today announced that the EMA has accepted the marketing authorisation ...

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FDA approves Biogen’s Tofidence (tocilizumab-bavi), a biosimilar referencing Actemra

29 September 2023 - Tofidence (BIIB800) becomes the first tocilizumab biosimilar to gain FDA approval in the US. ...

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Japanese regulator OKs Celltrion's Humira biosimilar

26 September 2023 - Celltrion said it has received marketing approval from the Japanese Ministry of Health, Labor, and Welfare ...

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Sandoz receives European Commission approval for Tyruko (natalizumab), first and only biosimilar for multiple sclerosis in Europe

26 September 2023 - Decision based on evidence from extensive analytical characterisation demonstrating similarity of biosimilar with reference biologic, in addition ...

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FDA issues complete response letter for Udencya Onbody biologics license application solely due to an on-going review of inspection findings at a third-party filler

25 September 2023 - No issues with clinical efficacy or safety, trial design, labeling, drug substance manufacturing, or device design or ...

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Biocon Biologics receives European Commission approval for Yesafili, biosimilar aflibercept

20 September 2023 - Biocon Biologics, a subsidiary of Biocon, has announced that the European Commission granted marketing authorisation in ...

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Alvotech provides US regulatory update on AVT02, a high concentration interchangeable biosimilar candidate to Humira (adalimumab)

20 September 2023 - Alvotech announced today that the US FDA has accepted Alvotech’s resubmitted biologics license application for AVT02, a ...

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Tyenne, Fresenius Kabi’s tocilizumab biosimilar, receives European Commission approval

19 September 2023 - Tyenne is the first tocilizumab biosimilar approved by the European Commission. ...

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Sandoz receives positive CHMP opinion for breast and gastric cancer biosimilar trastuzumab

18 September 2023 - Positive CHMP opinion based on comprehensive package of analytical, pre-clinical and clinical data. ...

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Inflation Reduction Act may accelerate generic and biosimilar market entry, but questions remain around CMS guidance

5 September 2023 - Last week, the Centers for Medicare and Medicaid Services announced its selection of the first 10 prescription ...

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