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  2. Biosimilar - Wikipedia

    en.wikipedia.org/wiki/Biosimilar

    The first biosimilar of a monoclonal antibody to be approved worldwide was a biosimilar of infliximab in the EU in 2013. [9] On March 6, 2015, the FDA approved the United States' first biosimilar product, the biosimilar of filgrastim called filgrastim-sndz (trade name Zarxio) by Sandoz.

  3. List of therapeutic monoclonal antibodies - Wikipedia

    en.wikipedia.org/wiki/List_of_therapeutic...

    This list of over 500 monoclonal antibodies includes approved and investigational drugs as well as drugs that have been withdrawn from market; consequently, the column Use does not necessarily indicate clinical usage. See the list of FDA-approved therapeutic monoclonal antibodies in the monoclonal antibody therapy page.

  4. US FDA approves two biosimilars for blockbuster eye drug Eylea

    www.aol.com/news/us-fda-approves-two-biosimilars...

    The agency approved Biocon Biologics' Yesafili as well as Samsung Bioepis and Biogen's Opuviz, while also allowing interchangeability, or the drug's substitution with biosimilars without the need ...

  5. Infliximab - Wikipedia

    en.wikipedia.org/wiki/Infliximab

    The FDA approved Samsung Bioepis Co., Ltd.'s Renflexis (infliximab-abda) in April 2017. [1] Biogen released another biosimilar, Flixabi, which was approved in Germany, the UK, and the Netherlands. [62] Flixabi was approved for use in the European Union in May 2016. [5] In December 2017, Ixifi (infliximab-qbtx) was approved in the United States. [4]

  6. US FDA proposes to remove switching study requirement for ...

    www.aol.com/news/us-fda-proposes-remove...

    Out of the 13 approved interchangeable biosimilars in the past, nine were approved without additional switching study data, the FDA said. KEY QUOTES "Both biosimilars and interchangeable ...

  7. Biologics Price Competition and Innovation Act of 2009

    en.wikipedia.org/wiki/Biologics_Price...

    The Biologics Price Competition and Innovation Act of 2009 (BPCI Act) amends the Public Health Service Act (PHS Act) to create an abbreviated approval pathway for biological products shown to be biosimilar to, or interchangeable with, an FDA-licensed reference biological product.

  8. US FDA approves Amgen's biosimilar to AstraZeneca's rare ...

    www.aol.com/news/us-fda-approves-amgens...

    Amgen's drug will be marketed under the name Bkemv. Biosimilars are close copies of complex biological drugs. In 2022, the company said that Bkemv met the main goal of a late stage study, where ...

  9. Biological therapy for inflammatory bowel disease - Wikipedia

    en.wikipedia.org/wiki/Biological_therapy_for...

    Instead there are biosimilars. Biosimilars are defined by the FDA as, "a biological product that is highly similar to and has no clinically meaningful differences from an existing FDA-approved reference product." [28] Currently, the only two biologic treatments for IBD that have approved biosimilars are adalimumab and infliximab. [11]