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The Vical influenza DNA vaccine is a plasmid-based vaccine platform developed by Vical Incorporated for pandemic preparedness and seasonal influenza. Formulated with the proprietary Vaxfectin adjuvant—a cationic lipid-based system (GAP-DMORIE/DPyPE)—the vaccine delivers DNA sequences encoding conserved and strain-specific influenza proteins, including hemagglutinin (HA), nucleoprotein (NP), and matrix protein 2 (M2). This approach is designed to elicit both neutralizing antibodies and broad T-cell mediated immunity. Developed under the RapidResponse program with support from the National Institute of Allergy and Infectious Diseases (NIAID), the vaccine aimed to provide a faster manufacturing alternative to traditional egg-based methods during pandemic outbreaks, such as H5N1 (avian flu). While clinical trials demonstrated safety and immunogenicity, the program was eventually deprioritized in favor of other pipeline candidates.
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