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BioSpace News Archive
Browse BioSpace’s published news and press releases by year, month, and day.
156 Results
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Deals
Press Release: Sanofi to acquire Inhibrx, Inc., adding potential best-in-class rare disease asset for Alpha-1 Antitrypsin Deficiency to pipeline
Sanofi and Inhibrx, Inc., a publicly traded clinical-stage biopharmaceutical company focused on developing a broad pipeline of novel biologic therapeutic candidates, have entered into a definitive agreement under which Sanofi has agreed to acquire Inhibrx following the spin-off of non-INBRX-101 assets into New Inhibrx.
January 23, 2024
·
10 min read
HEPHAISTOS-Pharma secures a €2 million seed round with xista science ventures, Foundation Fournier-Majoie and Noshaq
HEPHAISTOS-Pharma, a biotechnology company developing next generation immunotherapies against cancer, announced that it has raised a €2 million seed round to finance GMP transfer and advance its lead candidate towards the clinic.
January 23, 2024
·
2 min read
Policy
FDA Grants Breakthrough Device Designation to Amadix´s preventive screening blood test for Colorectal Cancer
Amadix, a Spanish biotech company, announced that PreveCol®, its colorectal cancer screening blood test, has received Breakthrough Device Designation from the U.S. Food and Drug Administration.
January 23, 2024
·
2 min read
FDA
AngioDynamics Announces FDA 510(k) Clearance of Auryon XL Radial Access Catheter to Treat Peripheral Arterial Disease
AngioDynamics Announces FDA 510(k) Clearance of Auryon XL Radial Access Catheter to Treat Peripheral Arterial Disease.
January 23, 2024
·
9 min read
Drug Development
Scholar Rock Announces FDA Clearance of IND Application to Initiate Phase 2 Proof-of-Concept Trial with Apitegromab to Treat Obesity
Scholar Rock Announces FDA Clearance of IND Application to Initiate Phase 2 Proof-of-Concept Trial with Apitegromab to Treat Obesity.
January 23, 2024
·
9 min read
Policy
Harbour BioMed Announces IND Clearance for HBM9027 in the U.S.
Harbour BioMed announced that the Company has been granted the clearance of Investigational New Drug from the Food and Drug Administration of the United States to initiate the first-in-human clinical trial in the U.S. for bispecific antibody HBM9027.
January 23, 2024
·
2 min read
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