08 DEC 2023 | US | FDA Approves First Cell-Based Gene Therapies Casgevy® and Lyfgenia® to Treat Sickle Cell Disease
The FDA approved Vertex/CRISPR Therapeutics’ Casgevy® and Blue...
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By Naomi Pearce | Dec 11, 2023
08 DEC 2023 | US | FDA Approves First Cell-Based Gene Therapies Casgevy® and Lyfgenia® to Treat Sickle Cell Disease
The FDA approved Vertex/CRISPR Therapeutics’ Casgevy® and Blue...
By Bioblast Editor | Dec 11, 2023
Celltrion USA announced that large Medical Benefits Manager Ventegra® will add Vegzelma®, Celltrion’s biosimilar to Genentech’s Avastin® (bevacizumab) on its commercial formulary as a preferred brand. Vegzelma® (bevacizumab-adcd) was approved by the FDA to treat six types o...
By Bioblast Editor | Dec 11, 2023
Lotus Pharmaceutical announced that it has entered into a partnership with Intas Pharmaceuticals for the commercialisation of Intas’s Prolia® (denosumab) biosimilar in South Korea, Taiwan and certain markets in South East Asia. According to the announcement, Intas will be ...
By Bioblast Editor | Dec 08, 2023
The FDA approved Vertex/CRISPR Therapeutics’ Casgevy® and Bluebird Bio’s Lyfgenia®, the first cell-based gene therapies to treat sickle cell disease in patients 12 years and older. Casgevy® is the first FDA-approved treatment that uses CRISPR/Cas9 to genetically modify a p...
By Bioblast Editor | Dec 08, 2023
Bio-Thera announced that its Avzivi® (BAT1706), biosimilar to Genentech’s Avastin® (bevacizumab) is FDA approved with a full indication set (excluding hepatocellular carcinoma). Bio-Thera is the only Chinese company to have received marketing approval for a biosimilar in t...
By Bioblast Editor | Dec 08, 2023
The National Institute for Health and Care Excellence (NICE) issued final draft guidance recommending AstraZeneca/MSD’s Lynparza® (olaparib) with bevacizumab be routinely used in the NHS in England and Wales for maintenance treatment of high-grade epithelial ovarian, ...
By Bioblast Editor | Dec 08, 2023
The US Patent Trial and Appeal Board (PTAB) has instituted Samsung Bioepis’ inter partes review (IPR) petition challenging Regeneron’s Eylea® (aflibercept) patent no. 10,464,992 in IPR proceeding IPR2023-01312. The patent claims formulations of aflibercept suitable for int...
By Bioblast Editor | Dec 08, 2023
The US Patent Trial and Appeal Board (PTAB) has instituted three of Samsung Bioepis’ inter partes reviews (IPR) petitions challenging Alexion’s Soliris® (eculizumab) patent nos. 9,725,504, 9,718,880 and 9,732,149 in IPR proceedings IPR2023-00999, IPR2023-00998 and IPR2023-0...
By Bioblast Editor | Dec 07, 2023
Bioeq and Teva jointly announced that Health Canada granted a Notice of Compliance for Ranopto® (ranibizumab), biosimilar to Genentech’s Lucentis® (ranibizumab). Ranopto® is indicated for the treatment of neovascular (wet) age-related macular degeneration, the treatment of...
By Bioblast Editor | Dec 07, 2023
Carefirst and another Blue Cross/Blue Shield licensee have brought class action proceedings against Johnson & Johnson (J&J) and Janssen alleging that the companies unlawfully delayed the introduction of biosimilar competition for its Stelara® ustekinumab product ont...
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