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In June 2017, Erelzi was approved for use in the European Union. [3] In March 2019, YLB113 (Etanercept biosimilar by YL Biologics) was approved in Japan. [61] In April 2019, Eticovo received FDA approval. [62] [63] In May 2020, Nepexto was approved for use in the European Union. [7] Rymti and Etera were approved for medical use in Australia in ...
This list of over 500 monoclonal antibodies includes approved and investigational drugs as well as drugs that have been withdrawn from market; consequently, the column Use does not necessarily indicate clinical usage.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.
Drug Trade name Type Main indications Company Sales (USD millions/year) ∆ vs 2014 1 Adalimumab: Humira Biologic Rheumatoid arthritis: AbbVie Inc. 14,012 1,469 2 Ledipasvir/sofosbuvir: Harvoni Small molecule Hepatitis C: Gilead Sciences: 13,864 11,737 3 Etanercept: Enbrel Biologic Rheumatoid arthritis: Amgen. Pfizer. 8,697 4,009 4 Infliximab ...
I would remind you that we have 100% success rate of FDA approval once we entered the clinic. And with 10 billion in cumulative biosimilar sales through '24, we're on track to double 2021 sales to ...
[77] [78] The brand name Humira stands for "human monoclonal antibody in rheumatoid arthritis", and was named by one of Abbott's employees, Richard J. Karwoski, who was also responsible for leading the effort to get Humira approved by the FDA. It is the third TNF inhibitor, after infliximab and etanercept, to be approved in the United States. [72]
The U.S. Food and Drug Administration (FDA) on Friday approved a new drug used for treating schizophrenia in adults, according to a press release. “This drug takes the first new approach to ...
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