Managing IP (MIP) has honoured Pearce IP as the only known ANZ IP firm founded by a woman. Separately, WEConnect International has certified Pearce IP as Women Owned.
CEO and ...
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By Pearce IP | Nov 14, 2023
Managing IP (MIP) has honoured Pearce IP as the only known ANZ IP firm founded by a woman. Separately, WEConnect International has certified Pearce IP as Women Owned.
CEO and ...
By Bioblast Editor | Nov 14, 2023
Alvotech and JAMP Pharma announced that Health Canada has granted marketing authorization for Jamteki™ (AVT04), the first approved biosimilar to Stelara® (ustekinumab) in Canada. AVT04 was developed by Alvotech and will be marketed under the name Jamteki® by JAMP in Canada...
By Bioblast Editor | Nov 14, 2023
Roche announced that the EU CHMP recommended the approval of its subcutaneous (SC) formulation of Tecentriq® (atezolizumab). The CHMP recommended Tecentriq SC for all indications for which Tecentriq® is approved, including various lung, liver, bladder and breast cancers.
By Bioblast Editor | Nov 14, 2023
AstraZeneca announced that China’s National Medical Products Administration (NMPA) approved its Imfinzi® (durvalumab) for the first-line treatment of adult patients with locally advanced or metastatic biliary tract cancer (BTC) in combination with chemotherapy (gemcitabine ...
By Bioblast Editor | Nov 13, 2023
Biocon Biologics announced that the UK Medicines and Healthcare products Regulatory Agency (MHRA) has approved its Yesafili®, biosimilar to Regeneron’s Eylea® (aflibercept), to treat neovascular age-related macular degeneration, visual impairment due to macular oedema secon...
By Bioblast Editor | Nov 13, 2023
The Korea Herald reported that Celltrion has confirmed in its phase III clinical trial that its omalizumab biosimilar CT-P39 is bioequivalent to Genentech/Novartis’ Xolair®. The company presented the final results of its 40 week clinical trial during the American College o...
By Naomi Pearce | Nov 13, 2023
10 NOV 2023 | EU | CHMP Positive Opinion for 8mg Eylea® (Aflibercept)
Bayer announced that the EMA’s Committee for Medicinal Products for Human Use (CHMP) has recommended approva...
By Bioblast Editor | Nov 10, 2023
Bayer announced that the EMA’s Committee for Medicinal Products for Human Use (CHMP) has recommended approval of 8mg Eylea® (aflibercept) intravitreal injection for the treatment of neovascular (wet) age-related macular degeneration (nAMD) and diabetic macular edema (DME), ...
By Bioblast Editor | Nov 10, 2023
Alvotech and its EU partner Stada announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) adopted a positive opinion for ustekinumab Uzpruvo (AVT04), biosimilar to Janssen’s Stelara®. This is the first positive CHMP o...
By Bioblast Editor | Nov 10, 2023
Lupin Limited announced that it has executed an agreement with the pharmaceutical manufacturer Amman Pharmaceuticals Industries for exclusive marketing and commercialisation of a biosimilar to Lucentis® (ranibizumab) in the middle east region, including Saudi Arabia and UAE...
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