FDA
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Crescent Biopharma Reports Third Quarter 2025 Financial Results and Recent Business Highlights
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Catalyst Biosciences (CBIO) Announces FDA Grants Catalyst Biosciences Orphan Drug Designation for MarzAA for the Treatment of Factor VII Deficiency
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Catalyst Biosciences Receives FDA Fast Track Designation for Subcutaneous MarzAA for the Treatment of Episodic Bleeding in Hemophilia A or B with Inhibitors
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Catalyst Biosciences (CBIO) Announces Pricing of 4.62M Public Offering of Common Stock at $6.50/sh
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Catalyst Biosciences Presents Positive Final Data from its Phase 2b Trial of Subcutaneous Dalcinonacog Alfa (DalcA) at the World Federation of Hemophilia Virtual Summit 2020
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Catalyst Biosciences Receives Patent in the European Union for Its Factor IX Portfolio
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Catalyst Biosciences Meets the Primary Endpoint of Reduction in Annualized Bleeding Rate in the Phase 2 Trial of Subcutaneous Marzeptacog Alfa (Activated) in Patients with Hemophilia A or B with Inhib
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