Samsung Bioepis AU Pty Ltd v Janssen Biotech, Inc. (Costs) [2024] FCA 1099
Stasiuk v Monster Energy Au Pty Ltd (No 3) [2024] FCA 1052
Rakman International Pty Limited v ...
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By Naomi Pearce, Helen Macpherson | Nov 19, 2024
Samsung Bioepis AU Pty Ltd v Janssen Biotech, Inc. (Costs) [2024] FCA 1099
Stasiuk v Monster Energy Au Pty Ltd (No 3) [2024] FCA 1052
Rakman International Pty Limited v ...
By Bioblast Editor | Nov 19, 2024
On 19 November 2024, Reuters reported that Novo Nordisk has launched Wegovy® (semaglutide) in China. The report states that sales will initially be made without insurance subsidy, although Novo Nordisk is investigating mechanisms to reduce costs for Chinese consumers.
...By Bioblast Editor | Nov 19, 2024
On 19 November 2024, the Economic Times reported that the Supreme Court of India has directed the Delhi High Court to move quickly on reconsidering an injunction, which was reinstated in October 2024, preventing Zydus from manufacturing, selling and marketing Sigrima™, bios...
By Bioblast Editor | Nov 19, 2024
On 19 November 2024, MSD (Merck in the US and Canada) announced positive topline results from its Phase 3 trial evaluating subcutaneous (SC) administration of pembrolizumab, together with Alteogen’s berahyaluronidase alfa, administered with chemotherapy. The SC pembrolizum...
By Bioblast Editor | Nov 19, 2024
On 19 November 2024, Xbrane and Intas announced they have entered an exclusive, global licensing and co-development agreement in relation to Xbrane´s nivolumab biosimilar candidate (referencing BMS’ Opdivo®). The biosimilar will be commercialised through Intas’ subsidiary ...
By Naomi Pearce, Helen Macpherson | Nov 19, 2024
QIP Nominees Pty Ltd. v Dana-Farber Cancer Institute, Inc. and The General Hospital Corporation [2024] APO 33
Date of decision:
07 August 2024
...
By Bioblast Editor | Nov 19, 2024
On 15 November 2024, Canada’s Drug Agency (CDA-AMC) published its final recommendation for Eli Lilly’s Ebglyss™ (lebrikizumab), recommending against reimbursement of Ebglyss™ by public drug plans, excluding Quebec, for the treatment of moderate-to-severe atopic dermat...
By Bioblast Editor | Nov 18, 2024
Regeneron has sued Sanofi, its partner in the commercialisation of the blockbuster eczema drug Dupixent® (dupilumab), in the US District Court for the Southern District of New York alleging that Sanofi is in breach of its commercialisation agreement. The issues relate to c...
By Naomi Pearce, Chantal Savage | Nov 18, 2024
Aflibercept
15 November 2024 | EU | Sandoz Aflibercept Biosimilars EU Approved & Formycon/Klinge Biosims Recommended
On 15 November 2024, Sandoz announced that its A...
By Bioblast Editor | Nov 18, 2024
On 18 November 2024, AbbVie announced that European Commission (EC) has approved Elahere® (mirvetuximab soravtansine) for the treatment of adult patients with folate receptor-alpha (FRα) positive, platinum-resistant high-grade serous epithelial ovarian, fallopian tube or pr...
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