Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
A personalized neoantigen vaccine platform developed by Washington University School of Medicine for the treatment of pediatric patients with recurrent or refractory brain tumors. The vaccine is tailored to each patient by identifying unique tumor mutations (neoantigens) through exome and cDNA-capture sequencing of tumor and normal tissue. It is designed to target up to 20 prioritized patient-specific neoantigens to stimulate a robust T-cell mediated immune response. The platform encompasses both polyepitope DNA plasmid vaccines, typically delivered via electroporation (e.g., using the TDS-IM v2.0 device), and synthetic long peptide vaccines. These vaccines are generally administered in combination with the adjuvant poly-ICLC (Hiltonol), a Toll-like receptor 3 (TLR3) agonist, to enhance dendritic cell activation and overall immunogenicity.
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 Personalized Neoantigen Vaccine (Washington University School of Medicine).