Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The human tyrosinase DNA vaccine is an experimental immunotherapy developed by Memorial Sloan Kettering Cancer Center for the treatment of melanoma. It consists of a pING plasmid vector encoding the human tyrosinase cDNA under the control of a cytomegalovirus (CMV) promoter. Tyrosinase is a key enzyme in melanin biosynthesis and serves as a melanosomal differentiation antigen that is highly expressed in most melanoma cells. By delivering the DNA sequence directly into host cells (typically via intramuscular injection), the vaccine aims to induce a specific T-cell mediated immune response against melanoma cells expressing the tyrosinase antigen. In clinical settings, this vaccine has been evaluated in Phase I trials, often administered in a sequential prime-boost strategy alongside a xenogeneic mouse tyrosinase DNA vaccine to enhance immunogenicity and overcome self-tolerance to the human protein.
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 human tyrosinase DNA vaccine.