Commonwealth of Australia v Sanofi [2024] HCA 47
Date of decision:
11 December 2024
Body:
High Court of Australia
Adjudicator:
Amgen’s BPCIA Denosumab Litigation Against Samsung Bioepis, Fresenius & Accord Centralised in New Jersey
By Bioblast Editor | Feb 06, 2025
On 6 February 2025, the US Judicial Panel on Multijurisdictional Litigation granted Amgen’s request to centralise its BPCIA litigation alleging that each of Samsung Bioepis, Fresenius Kabi and Accord Biopharma are infringing US patents covering Amgen’s Prolia® and Xgeva® (d...
Out to Pasture: Delayed Injunction Application Fails in Veterinary Patent Battle
By Naomi Pearce, Helen Macpherson | Feb 06, 2025
Abbey Laboratories Pty Ltd v Virbac (Australia) Pty Ltd [2024] FCA 1488
Date of decision:
17 December 2024
Body:
Federal Court of Austra...
Shanghai Henlius and Dr Reddy’s Enter Licence Agreement for Biosimilar Daratumumab
By Bioblast Editor | Feb 06, 2025
On 6 February 2025, Shanghai Henlius announced that it has entered into a licence agreement with Dr. Reddy’s for HLX15, biosimilar to Johnson & Johnson’s Darzalex® (daratumumab) and Darzalex Faspro® (daratumumab and hyaluronidase-fihi), used in treating multiple myeloma...
Novo Nordisk's Sales Increase 26% in 2024, Led by 56% Growth in Wegovy®/Saxenda®
By Bioblast Editor | Feb 05, 2025
On 5 February 2025, Novo Nordisk released its financial results for 2024, reporting a 26% sales increase (at constant exchange rates (CER)) to DKK 128.3 billion. Sales in Novo Nordisk’s diabetes care segment (including Ozempic® (semaglutide), Rybelsus® (oral semaglutide) a...
Henlius’ Serplulimab Becomes EU’s First Anti PD-1 mAb Approved for ES-SCLC
By Bioblast Editor | Feb 05, 2025
On 5 February 2025, Shanghai Henlius Biotech announced that Hetronifly® (serplulimab) was approved by the European Commission for use in combination with carboplatin and etoposide as a first line treatment of adult patients with extensive-stage small cell lung cancer (ES-SC...
Klinge and Lotus Pharma Partner to Commercialise Aflibercept Biosimilar in Key APAC Countries
By Bioblast Editor | Feb 05, 2025
On 5 February 2025, Formycon announced that its partner, Klinge Biopharma, has entered an exclusive licence agreement with Taiwan-based Lotus Pharmaceutical for the commercialisation of FYB203/Ahzantive®, biosimilar to Regeneron’s Eylea® (aflibercept) in the following Asia ...
Cytiva Subsidiary Seeks to Quash Subpoena Issued in Amgen’s US Denosumab Litigation Against Fresenius Kabi
By Bioblast Editor | Feb 04, 2025
On 4 February 2025, Cytiva subsidiary media supplier HyClone Laboratories filed a motion in the US District Court for the District of Utah, seeking to quash a subpoena issued to it by Amgen in the context of denosumab BPCIA patent infringement litigation Amgen commenced aga...
Permit Required: Full Court Denies Access to Costs Appeal in Carpark Patent Saga
By Naomi Pearce, Helen Macpherson | Feb 04, 2025
Vehicle Monitoring Systems Pty Limited v SARB Management Group Pty Ltd trading as Database Consultants Australia (Costs) [2024] FCAFC 155
Date of decision:<...
New Indication Alert: FDA Approves Genentech’s Susvimo® (Ranibizumab) for DME
By Bioblast Editor | Feb 04, 2025
On 4 February 2025, Genentech (a member of the Roche group) announced that the US FDA approved a new indication for Susvimo® (ranibizumab, 100mg/ml injection). Susvimo® is the first and only approved continuous delivery treatment for diabetic macular oedema (DME), the lead...
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