Celltrion USA announces US FDA approval of Zymfentra (infliximab-dyyb), the first and only subcutaneous infliximab, for the treatment of people with inflammatory bowel disease

22 October 2023 - Zymfentra is the first and only FDA approved subcutaneous formulation of infliximab approved for the maintenance treatment ...

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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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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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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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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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Outlook Therapeutics provides regulatory update on FDA review of ONS-5010 / Lytenava (bevacizumab-vikg) for the treatment of wet AMD

30 August 2023 - FDA issues complete response letter for ONS-5010 biologics license application based on CMC and need for further ...

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FDA approves first biosimilar to treat multiple sclerosis

24 August 2023 - The US FDA today approved Tyruko (natalizumab-sztn), the first biosimilar to Tysabri (natalizumab) injection for the treatment ...

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Dr. Reddy’s proposed rituximab biosimilar application accepted for review by US FDA, EMA and MHRA

12 July 2023 - Following dossier submission in April 2023, the regulatory agencies have now accepted the dossier for review. ...

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Express Scripts adds three biosimilars to largest formulary to promote competition and advance affordability, choices for patients

11 July 2023 - Express Scripts will include Cyltezo and both Sandoz products (Hyrimoz and unbranded adalimumab-adaz) – inflammatory disease biosimilars ...

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Idacio (adalimumab-aacf) now available in the United States

3 July 2023 - CMS grants Fresenius Kabi permanent, product-specific Q Code for Idacio (adalimumab-aacf). ...

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After five years of successful experience internationally, Biocon Biologics’ Hulio biosimilar to Humira, now available in the United States

3 July 2023 - Biocon Biologics today announced that Hulio (adalimumab-fkjp) injection, a biosimilar to Humira (adalimumab), is now available ...

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