Originally published in the IAM Saturday Opinion on 11 September 2021.
Australia was recently thrust into the global IP limelight when the Federal Court controversially determ...
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By Pearce IP | Sep 21, 2021
Originally published in the IAM Saturday Opinion on 11 September 2021.
Australia was recently thrust into the global IP limelight when the Federal Court controversially determ...
By Naomi Pearce | Sep 20, 2021
13 Sep 21 | Samsung Bioepis reported on a five-year follow-up study comparing ONTRUZANT® (trastuzumab biosimilar) with reference trastuzumab in early or locally advanced HER2 positi...
By Bioblast Editor | Sep 20, 2021
180 Life Sciences and Celltrion announced that they have entered into a Memorandum of Understanding for the supply of an anti-TNF biosimilar drug to be used for new indications with significant unmet medical needs.
By Bioblast Editor | Sep 20, 2021
AbbVie announced it has submitted the regulatory application for Skyrizi® (risankizumab) to the FDA for the treatment of patients 16 years and older with moderate to severe Crohn’s Disease.
By Bioblast Editor | Sep 20, 2021
Samsung Bioepis and Biogen announced that the FDA has approved Byooviz® (biosimilar ranibizumab) for the treatment of neovascular (wet) age-related macular degeneration, macular edema and myopic choroidal neovascularisation.
By Bioblast Editor | Sep 18, 2021
Henlius announced that it will present the results of new studies on serplulimab (anti-PD-1 mAb) and HLX04 (bevacizumab biosimilar) at the 24th Annual Meeting of Chinese Society of Clinical Oncology (CSCO).
By Bioblast Editor | Sep 18, 2021
Celltrion announced that South Korea’s MFDS has approved regdanvimab for the extended use in elderly patients aged 50 years and over, or with at least one underlying medical condition with mild symptoms of COVID-19, and in adults patients with moderate symptoms of COVID-19....
By Bioblast Editor | Sep 18, 2021
MSD announced that the first results from Ph III trials of Keytruda® (pembrolizumab) showed a statistically significant and clinically meaningful improvement in recurrence-free survival compared to placebo in patients with resected high-risk stage II melanoma.
By Bioblast Editor | Sep 17, 2021
Alvotech announced that the EU’s CHMP has adopted a positive opinion recommending the approval of AVT02 (proposed adalimumab biosimilar).
By Naomi Pearce | Sep 13, 2021
02 Sep 21 | US | Amgen and Hospira appear ready to settle the ongoing dispute relating to Neupogen® (filgrastim). The matter was due to go to a jury trial on 20 September 2021.
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