Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
VRC-FLUDNA061-00-VP is an investigational trivalent DNA vaccine developed by the National Institute of Allergy and Infectious Diseases (NIAID) Vaccine Research Center (VRC) for the prevention of seasonal influenza. The vaccine consists of three closed-circular plasmid DNA macromolecules (VRC-9328, VRC-2439, and VRC-9323) in equal amounts by weight. These plasmids encode the hemagglutinin (HA) sequences for three influenza strains matching the 2011/12 licensed inactivated influenza vaccine: A/California/04/2009 (H1N1), A/Perth/16/2009 (H3N2), and B/Brisbane/60/2008. Expression of the HA antigens is driven by a CMV/R promoter. As a DNA vaccine, it works by delivering plasmid DNA into human cells, which then produce the influenza proteins to act as antigens and stimulate an immune response. It has been evaluated in Phase 1b clinical trials (VRC 701) as a prime vaccination followed by a trivalent inactivated vaccine (TIV) boost to enhance the breadth and durability of the immune response 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 VRC-FLUDNA061-00-VP (Leidos Biomedical Research).