MPP’s Guide To Cutting Biosimilar Approval Times, Costs By Third Or More

Keytruda Biosim Could Cost 44% Less To Develop

The Medicines Patent Pool has conducted a study on the impact of licensing and technology transfer on the timeline and costs of developing five biosimilars, including Merck’s Keytruda. While a licensing deal for pembrolizumab might not be a near-term possibility, the findings could help licensors, licensees and regulators increase access to medicines.

The Three As Available Accessible Accordable
The Three A's Of Ideal Healthcare That MPP Strives To Achieve • Source: Shutterstock

It may be possible to achieve a 44% drop in the estimated development cost, and a 36% drop in the estimated timeline, for developing a biosimilar to Merck & Co’s checkpoint inhibitor Keytruda (pembrolizumab), shows a paper by authors from the Medicines Patent Pool.

While the figures are higher for a biosimilar to Roche’s monoclonal antibody Herceptin (trastuzumab) - 69% and 38% respectively...

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

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

 
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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.

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

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