by April Breyer Menon | May 21, 2024
On May 20, 2024, the FDA approved the first two interchangeable biosimilars of Regeneron’s EYLEA® (aflibercept) – Biocon Biologics and Mylan’s Yesafili™ (aflibercept-jbvf) and Samsung Bioepis’s Opuviz™ (aflibercept-yszy). There are at...
by April Breyer Menon | May 16, 2024
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by April Breyer Menon | May 8, 2024
According to a May 1, 2024 press release, the high-concentration (100 mg/mL), citrate-free formulation of Boehringer Ingelheim’s Cyltezo® (adalimumab-adbm) was approved by the FDA on May 1 as interchangeable with AbbVie’s Humira® (adalimumab) to treat multiple chronic...
by April Breyer Menon | May 3, 2024
On April 16, 2024, the PTAB proposed new rules (“proposed rules”) governing the Director Review process, which would remain consistent with the Interim review process currently in place, and codify those procedures. The types of cases available for Director Review...
by April Breyer Menon | May 3, 2024
First Actemra® Biosimilar Launch – Fresenius Kabi’s Tyenne® (tocilizumab-aazg) On April 15, 2024, Fresenius Kabi announced the U.S. launch of Tyenne® (tocilizumab-aazg), the first Actemra® (tocilizumab) biosimilar to launch in the U.S., after receiving FDA approval in...