FDA Approves Biocon’s Avastin® Biosimilar Jobevne™ (bevacizumab-nwgd)

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On April 10, 2025, Biocon announced the FDA approval of Jobevne™ (bevacizumab-nwgd) as the sixth biosimilar of Genentech’s Avastin® (bevacizumab). Jobevne™’s approval comes five years after its aBLA acceptance was publicly announced and joins Amgen / Allergan’s Mvasi® (bevacizumab-awwb), approved in September 2017, Pfizer’s Zirabev® (bevacizumab-bvzr), approved in June 2019, Amneal / mAbxience’s Alymsys® (bevacizumab-maly), approved in April 2022, Celltrion’s Vegzelma® (bevacizumab-adcd), approved in September 2022, and Bio-Thera’s Avzivi® (bevacizumab-tnjn), approved in December 2023. There are at least two pending aBLAs for Avastin® biosimilars, Samsung Bioepis’s SB8 and Centus / Fujifilm Kyowa Kirin’s FKB238, both accepted by the FDA in November 2019. Currently, there are no pending patent disputes related to Avastin® biosimilars.

According to a Q1 2025 Biosimilar Market Dynamics Report from Samsung Bioepis, Avastin® biosimilars have captured approximately 90% market share in the six years since the first launch and have discounts averaging 49% off the reference product’s average sale price (ASP).

Sales of bevacizumab were approximately $2 billion in 2023.

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The author would like to thank April Breyer Menon for her contributions to this article.

DISCLAIMER: Because of the generality of this update, the information provided herein may not be applicable in all situations and should not be acted upon without specific legal advice based on particular situations. Attorney Advertising.

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