Dynavax announces FDA acceptance for review of biologics license application and PDUFA action date for Heplisav-B

30 March 2016 - Dynavax Technologies Corporation announced today that the U.S. FDA has accepted for review the biologics license application for Helplisav-B, the company's vaccine candidate for immunization against hepatitis B infection in adults 18 years of age and older. The FDA has established September 15, 2016 as the Prescription Drug User Fee Act action date.

For more details, go to: http://investors.dynavax.com/releasedetail.cfm?ReleaseID=962813

Michael Wonder

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Michael Wonder

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US , Vaccine , Dossier