Australian Mud Company Pty Ltd v Globaltech Corporation Pty Ltd & Ors (No 2) [2022] FCA 88(experimental evidence) Australian Mud Company Pty Ltd & Anr v Globaltech Corporati...
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By Naomi Pearce | May 24, 2022
Australian Mud Company Pty Ltd v Globaltech Corporation Pty Ltd & Ors (No 2) [2022] FCA 88(experimental evidence) Australian Mud Company Pty Ltd & Anr v Globaltech Corporati...
By Bioblast Editor | May 24, 2022
Alpine Immune Sciences announced that the FDA has removed the partial clinical hold placed on its NEON-2 trial evaluating davoceticept (first-in-class conditional CD28 costimulator and dual checkpoint inhibitor) in combination with pembrolizumab in adults with advanced mali...
By Bioblast Editor | May 24, 2022
The UK’s NICE published final draft guidance recommending Vabysmo® (faricimab) for the treatment of adult patients with wet age-related macular degeneration (AMD) or diabetic macular oedema (DMO).
By Bioblast Editor | May 24, 2022
Shanghai Henlius Biotech announced that it has entered into a semi-exclusive license agreement with Abbott Operations Uruguay for the commercialisation of Hanlikang® (biosimilar rituximab) and Hanquyou® (biosimilar trastuzumab) in Brazil.
By Naomi Pearce | May 23, 2022
Jusand Nominees Pty Ltd v Rattlejack Innovations Pty Ltd [2022] FCA 540
Date:
Court:
Judge:
16 May 2022
Federal Court of Aust...
By Bioblast Editor | May 23, 2022
Biond Biologics announced the first patients have been dosed in its Ph I trials of BND-22 (an Ig-Like Transcript 2 (ILT2) receptor blocking antibody) in combination with pembrolizumab or cetuximab being conducted in Israel and the US. BND-22 is being developed under an exc...
By Bioblast Editor | May 23, 2022
The US District Court of Delaware has set down BMS’ patent infringement case against AstraZeneca regarding Imfinzi® (durvalumab) as a jury trial in April 2024. BMS filed a complaint against AstraZeneca in March 2022, alleging that AstraZeneca’s Imfinzi® (durvalumab) infrin...
By Bioblast Editor | May 20, 2022
MSD announced that it has received a positive opinion from the CHMP for its anti-PD-1 therapy Keytruda® (pembrolizumab) as monotherapy for the adjuvant treatment for adult and adolescent patients with stage IIB or IIC melanoma following complete resection. CHMP additional...
By Bioblast Editor | May 20, 2022
The CHMP recommended refusing the marketing authorisations for Prestige Biopharma’s applications for trastuzumab biosimilars Tuznue® and Hervelous®. The CHMP stated that the manufacturing process used for the commercial production of these medicines differed from that used...
By Bioblast Editor | May 19, 2022
Biocon Biologics and Viatris announce the launch of Abevmy® (biosimilar bevacizumab) in Canada. Abevmy® was jointly developed by Biocon Biologics and Viatris, and is indicated for metastatic colorectal cancer, locally advanced, metastatic or recurrent non-small cell lung c...
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