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Biotech / Medical : biotech firesales

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From: Julius Wong	4/27/2016 9:12:17 AM
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BERKELEY, CA--(Marketwired - April 27, 2016) - Dynavax Technologies Corporation ( DVAX) today announced that the U.S. Food and Drug Administration (FDA) will require additional time to complete its review of the Biologics License Application (BLA) for HEPLISAV-B™, Dynavax's investigational vaccine for immunization of adults against hepatitis B infection. In a notice received from the FDA, the Prescription Drug User Fee Act (PDUFA) action date for HEPLISAV-B has been extended by three months to December 15, 2016.

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