Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The Vaxfectin-formulated trivalent influenza DNA vaccine is a plasmid DNA-based vaccine developed by Vical Incorporated for the prevention of influenza, specifically targeting highly pathogenic avian influenza strains such as H5N1. The vaccine consists of three distinct plasmids encoding the H5 hemagglutinin (HA), nucleoprotein (NP), and matrix protein 2 (M2) of the influenza virus. It is formulated with Vaxfectin, a proprietary cationic lipid-based adjuvant designed to enhance the delivery of the plasmid DNA into host cells and significantly boost both humoral (antibody) and cellular (T-cell) immune responses. By including conserved internal proteins like NP and M2 alongside the surface HA protein, the vaccine was intended to provide broader and more durable protection against drifting or pandemic influenza strains compared to traditional seasonal vaccines. Clinical development reached Phase 1, where the vaccine demonstrated safety and the ability to induce multi-antigenic immune responses in healthy adults.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on Vaxfectin-formulated trivalent influenza DNA vaccine.