by April Breyer Menon | Mar 31, 2026
On March 30, 2026, the FDA approved Teva’s biosimilar Ponlimsi™ (denosumab-adet), referencing Amgen’s Prolia® (denosumab), for all indications of the reference product. Ponlimsi™ is the tenth Prolia® / Xgeva® (denosumab) biosimilar approved by the FDA....
by April Breyer Menon | Mar 26, 2026
On March 20, 2026, Accord, Intas, and Bio-Thera Solutions filed four petitions for inter partes review (“IPR”) challenging Janssen patents related to Simponi® (golimumab). The petitions are IPR2026-00256 (U.S. Patent No. 11,014,982 (“the ’982 patent”)), IPR2026-00257...
by April Breyer Menon | Mar 12, 2026
On March 9, 2026, the FDA updated its guidance addressing biosimilar development under the Biologics Price Competition and Innovation Act (BPCIA) (“New and Revised Draft Q&As on Biosimilar Development and the BPCI Act (Revision 4)”). These updates follow the FDA’s...
by April Breyer Menon | Mar 10, 2026
Download PDF Download...
by April Breyer Menon | Mar 6, 2026
On March 3, 2026, Janssen filed a Complaint in the U.S. District Court for the District of Delaware against Accord and Bio-Thera Solutions, Case No. 1:26-cv-00222 (D. Del.), initiating the first BPCIA litigation related to Janssen / Johnson &...