Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The heterologous HER2 DNA vaccine is an investigational therapeutic cancer vaccine platform designed to overcome immune tolerance to self-antigens in HER2-expressing malignancies, such as breast cancer. This vaccination strategy typically utilizes DNA plasmids encoding xenogeneic (heterologous) HER2 sequences (such as human HER2, rat Neu, or hybrid human/rat HER2 constructs), often delivered via intramuscular injection combined with electroporation. By presenting a slightly foreign (heterologous) version of the HER2 antigen, the vaccine breaks immunological tolerance and stimulates robust, cross-reactive humoral and cellular (T-cell) immune responses against self-HER2 overexpressed on tumor cells. Some specific candidates within this class, such as VM206RY, employ a heterologous prime-boost regimen combining a DNA plasmid primer with a recombinant adenoviral vector boost to further enhance antigen-specific immunity.
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 heterologous HER2 DNA vaccine.