
Huiya Wu
Articles
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Jan 2, 2025 |
jdsupra.com | Huiya Wu
On October 24, 2014, Amgen initiated the first litigation under the Biologics Price Competition and Innovation Act (“BPCIA”), asserting infringement of two patents. Over the last two calendar years, Amgen, Biogen, Genentech, and Regeneron have all filed BPCIA complaints (sometimes several) asserting 20 or more patents.
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Nov 13, 2024 |
mondaq.com | David Chen |Huiya Wu |Kristopher Brown |Krystal J. Lin
Goodwin is presenting a two-part publication series covering life sciences trends involving license deals, M&A, and financing for Greater China's life sciences sector. See the first post in the series here. While the overall Chinese M&A market fluctuated from 2021 to 2023 due to the pandemic and other factors, the life sciences pharmaceutical and biotech market remained relatively stable. Though the number of deals dipped in 2022, in 2023, it quickly recovered to 2021 levels.
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May 20, 2024 |
mondaq.com | Huiya Wu
we previously reported, in May 2023, Amgen filed a BPCIA complaint in the District of New Jersey alleging infringement based on Sandoz's denosumab biosimilars of Amgen's PROLIA and XGEVA ("the Sandoz Denosumab Litigation"). The FDA subsequently, in March 2024, approved Sandoz's denosumab biosimilars, WYOST (denosumab-bbdz) and JUBBONTI (denosumab-bbdz), as interchangeable with Amgen's XGEVA and PROLIA products.
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May 16, 2024 |
jdsupra.com | Huiya Wu
As we previously reported, in May 2023, Amgen filed a BPCIA complaint in the District of New Jersey alleging infringement based on Sandoz’s denosumab biosimilars of Amgen’s PROLIA and XGEVA (“the Sandoz Denosumab Litigation”). The FDA subsequently, in March 2024, approved Sandoz’s denosumab biosimilars, WYOST (denosumab-bbdz) and JUBBONTI (denosumab-bbdz), as interchangeable with Amgen’s XGEVA and PROLIA products.
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May 15, 2024 |
bigmoleculewatch.com | Huiya Wu
As we previously reported, in May 2023, Amgen filed a BPCIA complaint in the District of New Jersey alleging infringement based on Sandoz’s denosumab biosimilars of Amgen’s PROLIA and XGEVA (“the Sandoz Denosumab Litigation”). The FDA subsequently, in March 2024, approved Sandoz’s denosumab biosimilars, WYOST (denosumab-bbdz) and JUBBONTI (denosumab-bbdz), as interchangeable with Amgen’s XGEVA and PROLIA products.
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