MSA 4×4 Accessories Pty Ltd v Clearview Towing Mirrors Pty Ltd [2024] FCA 24
Date: 24 January 2024
Court: Federal Court
Judge: Downes J
Date:...
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By Helen Macpherson, Naomi Pearce | Feb 28, 2024
MSA 4×4 Accessories Pty Ltd v Clearview Towing Mirrors Pty Ltd [2024] FCA 24
Date: 24 January 2024
Court: Federal Court
Judge: Downes J
Date:...
By Bioblast Editor | Feb 27, 2024
On 27 February 2024, Akeso announced results of a Phase II clinical trial for cadonilimab combined with standard treatment (chemotherapy +/- bevacizumab) for treating recurrent/metastatic cervical cancer. The results were published in the American Association for Cancer Re...
By Bioblast Editor | Feb 27, 2024
On 27 February 2024, AbbVie announced that the U.S. Food and Drug Administration (FDA) granted priority review of its supplemental Biologics License Application for EPKINLY® (epcoritamab) for the treatment of Adult Relapsed or Refractory Follicular Lymphoma (R/R FL). Prior...
By Bioblast Editor | Feb 27, 2024
On 27 February 2024, BeiGene, announced that the U.S. Food and Drug Administration (FDA) accepted BeiGene’s Biologics License Application (BLA) for TEVIMBRA® (tislelizumab), in combination with fluoropyrimidine-and platinum-containing chemotherapy, with a PDUFA date s...
By Bioblast Editor | Feb 26, 2024
On 26 February 2024, AstraZeneca announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency has recommended the use of Voydeya® (danicopan) as an add-on to ravulizumab or eculizumab for the treatment of adult patients with paro...
By Bioblast Editor | Feb 26, 2024
On 26 February 2024, BeiGene announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has issued a positive opinion recommending the approval of TEVIMBRA® (tislelizumab) for the treatment of non-small cell lung cancer (...
By Bioblast Editor | Feb 26, 2024
On 26 February 2024, the results of an 18 month study sponsored by Takeda Pharmaceuticals were published in Crohn’s & Colitis 360. The study involved 108 patients switched from IV to a subcutaneous vedolizumab. The results of the study suggested that switching f...
By Naomi Pearce, Chantal Savage | Feb 26, 2024
23 FEB 2024 | EU | Samsung Bioepis Presented Study Results for ustekinumab SB17, Biosimilar to Janssen’s Stelara®, at ECCO
On 23 February 2024, Samsung Bioepis presented two new ...
By Bioblast Editor | Feb 26, 2024
On 26 February 2024, Daily Pharm Korea reported that Samsung Bioepis received approval from the Korean Ministry of Food and Drug Safety for Afilivu®, biosimilar to Regeneron’s Eylea® (aflibercept). This is the first aflibercept biosimilar approved in Korea and Samsung Bioe...
By Bioblast Editor | Feb 26, 2024
On 26 February 2024, Alvotech announced the sale of 10,127,132 ordinary shares at a purchase price of USD 16.41 per share. Alvotech’s U.S listed shares rose more than 12% to $18 in premarket trading following the announcement on 23 February 2024 that FDA approved Alv...
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