Bioverativ Announces FDA Acceptance of Investigational New Drug Application for BIVV001 to Treat Hemophilia A
BIOVERATIV INC COMMON (BIVV)
Last bioverativ inc common earnings: 2/13 04:15 pm
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Source: Business Wire
BIVV001 is a novel, investigational factor VIII therapy designed to extend protection from bleeds with prophylaxis dosing of once weekly or longer On track to initiate a Phase 1/2a clinical trial in the second half of 2017 WALTHAM, Mass.--(BUSINESS WIRE)-- Bioverativ (NASDAQ: BIVV), a global biotechnology company focused on the discovery, development and commercialization of innovative therapies for hemophilia and other rare blood disorders, today announced that the U.S. Food and Drug Administration (FDA) has accepted the company’s Investigational New Drug (IND) application for BIVV001 (also known as rFVIIIFc-VWF-XTEN), a novel, investigational factor VIII therapy designed to potentially extend protection from bleeds with prophylaxis dosing of once weekly or longer for people with hemophilia A. “People with hemophilia A continue to have a strong unmet need f
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