More Stelara Biosimilars Line Up For Launch In US And EU

Samsung Bioepis And Sandoz Win US Ustekinumab Approval As Celltrion Endorsed By EMA

Samsung Bioepis and partner Sandoz have won approval for a third US Stelara biosimilar. Meanwhile, in Europe Celltrion has become the latest firm to qualify for an ustekinumab marketing authorization.

EU and US flags
More Stelara biosimilars have been endorsed by EU and US regulators • Source: Shutterstock

More biosimilar rivals to Stelara (ustekinumab) are on the way on both sides of the Atlantic, after the US Food and Drug Administration and European Medicines Agency separately endorsed products from major players that are aiming to imminently compete in what promises to be a lucrative market.

Stelara brought in $10.858bn for Johnson & Johnson in 2023, up 11.7% over 2022’s $9.723bn. In the US, sales grew...

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An abbreviated licensure pathway for biologics was created by the 2009 Biologics Price Competition and Innovation Act. Biologics demonstrated to be biosimilar to or interchangeable with FDA-approved products can use the 351(k) biologics license application pathway. Biosimilars BLAs submitted under the 351(k) pathway have a 12 month user fee goal for FDA action. Updated weekly.

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