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WSJ.com: US Business, Wall Street Journal: Business
Fri, 03/06/2015 - 7:30am

The FDA approved its first “biosimilar” drug, a decision expected to launch a new industry of lower-cost versions of expensive drugs that could help the U.S. curb its $300 billion in yearly drug spending.

Topics: fda u.s biosimilar drug

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FDA approves Boehringer Ingelheim’s Cyltezo for inflammatory ailments
The US Food and Drug Administration (FDA) has approved Boehringer Ingelheim's high-concentration, citrate-free formulation of Cyltezo (adalimumab-adbm), an interchangeable biosimilar to Humira ...
05/1/2024 - 9:31 pm | View Link
FDA Approves High-Concentration Cyltezo
The FDA approved a high-concentration, citrate-free version of Boehringer Ingelheim’s Cyltezo (adalimumab-adbm), making it the second high-concentration adalimumab biosimilar to have an ...
05/1/2024 - 8:43 am | View Link
FDA Approves New Herceptin Biosimilar for the Treatment of Multiple HER2-Overexpressing Cancers
Hercessi marks Accord BioPharma’s first biosimilar to be approved in the United States, with multiple indications for HER2-overexpressing breast and gastric cancers.
04/29/2024 - 6:28 am | View Link
FDA Approves Hercessi, the Sixth Trastuzumab Biosimilar
The recent FDA approval of Hercessi expands access to a treatment previously burdened by high costs. Hercessi joins the 5 other biosimilars already on the market.
04/29/2024 - 5:02 am | View Link
FDA Approves Henlius’ Trastuzumab Biosimilar, Hercessi
The approval marks the sixth for a biosimilar referencing Herceptin (trastuzumab) for the treatment of HER2-positive breast and gastric cancers.
04/29/2024 - 2:59 am | View Link
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