A $31bn Opportunity? Future Of Biosimilars Inches Closer With Samsung Keytruda Study

Kick Off For Samsung Phase I Study Follows Recent Phase III News From Sandoz

Samsung Bioepis is among a small pool of players heading to the clinic for a proposed biosimilar to Merck & Co’s PD-1 mega-blockbuster, as interest and investment rises ahead of patent expiry at the end of the decade.

Samsung Bioepis has kicked off a Phase I clinical study for its SB27 biosimilar Keytruda (pembrolizumab) candidate, putting another player in the race to develop competition to the definitive immuno-oncology powerhouse that has been tipped to generate sales of $31bn by the time biosimilars roll around at the end of the current decade.

The Korean firm’s study will compare the pharmacokinetics, efficacy, safety, and immunogenicity of SB27 versus EU-sourced and US-sourced Keytruda, in...

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

 
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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.

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Biocon And Teva Sign Up To Biosimilars Forum

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