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3 July 2015Americas

Biosimilars market value could triple by 2020, says report

The market value for biosimilars around the world could reach $20 billion by the end this year and that figure could nearly triple by 2020, according to a report.

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More on this story

Europe
The plausibility battleground at the EPO
9 November 2020   Plausibility in the context of the inventive step and sufficiency requirements can be a contentious issue before the European Patent Office. Markus Grammel of Grünecker reports.
Americas
US FDA approves first biosimilar, keeps quiet on naming standards
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More on this story

Europe
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9 November 2020   Plausibility in the context of the inventive step and sufficiency requirements can be a contentious issue before the European Patent Office. Markus Grammel of Grünecker reports.
Americas
US FDA approves first biosimilar, keeps quiet on naming standards
9 March 2015   The US Food and Drug Administration approved Sandoz’s cancer product Zarxio on Friday—the first biosimilar to be rubber stamped in the US.
Biotechnology
Association calls for more biosimilar cancer therapies in Europe
11 October 2018   Cancer biosimilars are slow to enter European drugs markets even after the branded products have gone off-patent, according to the Association of European Cancer Leagues.

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