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Takeda and HUTCHMED Announce FDA New Drug Application (NDA) for Fruquintinib
Friday, May 26, 2023Takeda and HUTCHMED announced that the US Food and Drug Administration FDA has granted priority review of the New Drug Application NDA for fruquintinib a highly selective and potent inhibitor of vascular endothelial growth factor receptors VEGFR an...
Pfizer Announces FDA Approval of PAXLOVID™ for Adult Patients
Friday, May 26, 2023Pfizer announced that the US Food and Drug Administration FDA has approved PAXLOVID nirmatrelvir tablets and ritonavir tablets for the treatment of mildtomoderate COVID in adults who are at high risk for progression to severe COVID including hospital...
Bristol Myers Squibb and Janssen Pharmaceuticals Collaborate to Receive FDA Fast Track Designation for Milvexian
Thursday, May 25, 2023Bristol Myers Squibb in collaboration with Janssen Pharmaceuticals announced that all three prospective indications for milvexian an investigational oral factor XIa FXIa inhibitor have now been granted Fast Track Designation by the US Food and Drug A...
Novo Nordisk Collaborates with Life Edit Therapeutics
Thursday, May 25, 2023Novo Nordisk and Life Edit Therapeutics announced a research and development collaboration to discover and develop gene editing therapies against a select set of therapeutic targets
CohBar and Morphogenesis Enter into Merger Agreement
Wednesday, May 24, 2023CohBar Morphogenesis announced that they have entered into a definitive agreement for an allstock transaction forming a company combining expertise and resources to advance a latestage oncology pipeline
Rocket Pharmaceuticals Receives FDA Regenerative Medicine Advanced Therapy (RMAT) Designation for RP-L301
Wednesday, May 24, 2023Rocket Pharmaceuticals announced that the US Food and Drug Administration FDA has granted Regenerative Medicine Advanced Therapy RMAT designation to RPL the investigational lentiviralbased gene therapy for Pyruvate Kinase Deficiency PKD a rare blood...
UCB Collaborates with Veeva Systems
Wednesday, May 24, 2023Rocket Pharmaceuticals announced that the US Food and Drug Administration FDA has granted Regenerative Medicine Advanced Therapy RMAT designation to RPL the investigational lentiviralbased gene therapy for Pyruvate Kinase Deficiency PKD a rare blood...
PharmAbcine Receives IND Approval from the Korean MFDS for Phase I Clinical Trial of Its Novel TIE2 Agonistic Antibody in nAMD
Wednesday, May 24, 2023PharmAbcine Inc KOSDAQ ks a clinicalstage biotech company focusing on the development of nextgeneration antibody therapeutics announced today that the Company received IND Investigational New Drug approval from the Korean MFDS Ministry of Food and Dr...
ClearPoint Neuro Enters into Licence Agreement with UCB
Wednesday, May 24, 2023ClearPoint Neuro announced that it has entered into a multiyear licence agreement with UCB to partner on drug delivery platforms for UCBs gene therapy portfolio
AbCellera Partners with the Governments of Canada and British Columbia
Wednesday, May 24, 2023AbCellera announced a CA million coinvestment with the Governments of Canada and British Columbia to build new capabilities and infrastructure to develop innovative antibodybased medicines and strengthen Canadas leadership in clinical research manufa...
