Following our recent announcement that Principal Naomi Pearce (Patent Star 2021) was honoured with a Managing IP (MIP) Patent Star 2021 awards, Pearce IP’s Special Counsel Patent At...
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By Pearce IP | Jun 25, 2021
Following our recent announcement that Principal Naomi Pearce (Patent Star 2021) was honoured with a Managing IP (MIP) Patent Star 2021 awards, Pearce IP’s Special Counsel Patent At...
By Bioblast Editor | Jun 25, 2021
UCB announced that the CHMP has recommended BIMZELX® (bimekizumab) for the treatment of plaque psoriasis.
By Bioblast Editor | Jun 25, 2021
Samsung Bioepis and Biogen announced that the CHMP has recommended BYOOVIZ™/SB11 (proposed ranibizumab biosimilar) for the treatment of neovascular (wet) age-related macular degeneration, visual impairment due to diabetic macular oedema, proliferative diabetic retinopathy, ...
By Naomi Pearce | Jun 25, 2021
Diagnostic tests that rely on a naturally occurring phenomenon patent eligible in Australia
On 18 June 2021, the Full Court of the Federal Court confirmed in Ariosa Diagnostic...
By Bioblast Editor | Jun 24, 2021
The CHMP recommended granting conditional marketing authorisation for Minjuvi® (tafasitamab) for the treatment of relapsed or refractory diffuse large B-cell lymphoma, and Abecma® (idecabtagene vicleucel) for the treatment of relapsed and refractory multiple myeloma.
By Bioblast Editor | Jun 24, 2021
The Committee for Medicinal Products for Human Use (CHMP) recommended expanding the indications for Opdivo® (nivolumab) and Rinvoq® (upadacitinib). If approved, Opdivo® will also be indicated for oesophageal or oesophageal junction cancer. If approved, Rinvoq® will also be ...
By Bioblast Editor | Jun 24, 2021
Health insurance provider Cigna announced it will offer a one-time US$500 payment to patients who switch to a biosimilar or another preferred medication. This payment will be provided in a debit card and can be spent on health care services and products.
By Bioblast Editor | Jun 23, 2021
Innovent Biologics announced its Ph III trials of sintilimab in combination with chemotherapy met the overall survival primary endpoint.
By Bioblast Editor | Jun 23, 2021
Genentech announced that the FDA has accepted the BLA for its Port Delivery System (PDS) with ranibizumab under Priority Review. Genentech is seeking approval for its PDS for the treatment of wet, or neovascular, age-related macular degeneration (AMD).
By Naomi Pearce | Jun 22, 2021
Date: 22 June 2021Forum: Australian Patent OfficeDelegate: Xavier Gisz
Background
As part of the Raising the Bar amendments introduced to the Patents Act 1990 (Cth) in ...
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