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

Keytruda Biosim Could Cost 44% Less To Develop

 
• By Vibha Ravi

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., Inc.’s checkpoint inhibitor Keytruda (pembrolizumab), shows a paper by authors from the Medicines Patent Pool (MPP).

While the figures are higher for a biosimilar to Roche Holding AG’s monoclonal antibody Herceptin (trastuzumab) - 69% and 38% respectively – the main patents on trastuzumab have expired

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