Pearce IP provides weekly reports on global biosimilars activities in the Pearce IP BioBlast®. Significant biosimilar activities for the week ending 8 August 2025 are set out below...
Home / Search Results
Stay informed about important legal and industry news with our blogs and weekly BioBlast® updates.
By Naomi Pearce, Chantal Savage | Aug 12, 2025
Pearce IP provides weekly reports on global biosimilars activities in the Pearce IP BioBlast®. Significant biosimilar activities for the week ending 8 August 2025 are set out below...
By Bioblast Editor | Aug 12, 2025
On 12 August 2025, Celltrion announced that it has been awarded a series of supply contracts in Italy for its autoimmune disease therapies and oncology treatments. Key contracts include additional contracts for Steqeyma®, biosimilar to J&J/Janssen’s Stelara® (ustekinum...
By Bioblast Editor | Aug 12, 2025
On 12 August 2025, Lupin announced that it has partnered with Sandoz to market and commercialise Lupin’s biosimilar ranibizumab (referencing Genentech’s Lucentis®) across the European Union (excluding Germany), Switzerland, Norway, Canada, Australia, Hong Kong, Vietnam, and...
By Bioblast Editor | Aug 12, 2025
On 12 August 2025, the Swiss Federal Patent Court upheld Samsung Bioepis’ invalidity action against the Swiss and Liechtenstein part of Janssen Biotech’s European Patent 3883606. Janssen’s ‘606 patent relates to the use of ustekinumab (the active ingredient in Stelara®) in...
By Bioblast Editor | Aug 11, 2025
On 11 August 2025, Australia’s Therapeutic Goods Administration (TGA) approved a new brand of Novartis’ ofatumumab:
ZOPHEOS ofatumumab 20 mg/0.4mL solution for injection pre-filled pen (490662)
ZOPHEOS ofatumumab 20 mg/0.4mL solution for injection pre-fille...
By Paul Johns | Aug 08, 2025
Pearce IP’s Head of Litigation New Zealand, Paul Johns, and our Head of Trade Marks discuss the third party “revival” of the ANSETT brand in 2025 for travel agency services, more than 20 years after the airline folded
By Bioblast Editor | Aug 07, 2025
On 7 August 2025, Sandoz announced that it is streamlining the clinical development programs for its nivolumab and ocrelizumab biosimilars, following “ongoing encouraging and favourable regulatory developments” and feedback from major regulatory authorities regarding the re...
By Bioblast Editor | Aug 06, 2025
On 6 August 2025, Celltrion announced that the US FDA has approved an expanded indication for its IV formulation of Avtozma®, biosimilar to Roche’s Actemra® (tocilizumab), for the treatment of cytokine release syndrome (CRS) in adults and paediatric patients aged 2 years an...
By Bioblast Editor | Aug 06, 2025
On 6 August 2025, Intas Pharmaceuticals, and its global subsidiaries operating under the Accord brand, announced the successful acquisition of Udenyca®, biosimilar to Amgen’s Neulasta® (pegfilgrastim), from Coherus Biosciences. The addition of Udenyca® expands Intas and Ac...
By Naomi Pearce, Chantal Savage | Aug 05, 2025
Pearce IP provides weekly reports on global biosimilars activities in the Pearce IP BioBlast®. Significant biosimilar activities for the week ending 1 August 2025 are set out below...
SUBSCRIBE TO PEARCE IP