US Lucentis Competition Expectations Upended By Byooviz

Ranibizumab Biosimilar Competition Had Been Expected By End Of 2021 In US

Samsung Bioepis’ indication that it will not launch its FDA-approved ranibizumab biosimilar, Byooviz, before June 2022 has changed what we know about the competitive landscape for Lucentis in the US.

2021 2022 Roll Over Wooden Blocks
Biosimilar competition to Lucentis has rolled over to 2022 • Source: Alamy

When Samsung Bioepis announced the recent US Food and Drug Administration approval of its Byooviz (ranibizumab-nuna) biosimilar, the first approved US rival to Genentech’s Lucentis, a key detail was revealed by the company that could reshape expectations about US biosimilar competition to the ophthalmic brand.

Celebrating the FDA’s first approval of a biosimilar with ophthalmic indications – with the product approved for the treatment of...

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UK Invests £28m In NHS AI, But Industry Says Procurement And Training Will Determine Success - C7

 
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The UK government has said it will invest almost £30m ($40.4m) in AI technologies to modernize the NHS and reduce wait times – but for the medtech sector, the devil will be in the details.

UK Invests £28m In NHS AI, But Industry Says Procurement And Training Will Determine Success - C6

 
• By 

The UK government has said it will invest almost £30m ($40.4m) in AI technologies to modernize the NHS and reduce wait times – but for the medtech sector, the devil will be in the details.

US Biosimilars

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.

Top 10 Drugs Q1 2026: New Sheriff In Town As Mounjaro Unseats Keytruda - Clone - Clone

Mounjaro, Eliquis, and Darzalex buck the Q1 trend to make gains

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Biocon And Teva Sign Up To Biosimilars Forum

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