Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This autologous dendritic cell vaccine is a biologic immunotherapy developed by the University of Louisville for the treatment of pediatric patients with relapsed or refractory high-grade gliomas, medulloblastomas, and central nervous system primitive neuroectodermal tumors (CNS PNETs). The vaccine is produced by harvesting a patient's own dendritic cells and pulsing them with peptides from specific tumor-associated antigens, namely NY-ESO-1, MAGE-A1, and MAGE-A3. These antigens are often expressed in pediatric brain tumors but are typically absent in normal tissues. The vaccine is designed to be administered in a combination regimen with decitabine, a hypomethylating agent used to upregulate antigen expression on tumor cells, and Hiltonol (poly-ICLC), a toll-like receptor 3 (TLR3) agonist that serves as an immune adjuvant to enhance the activation and recruitment of T-cells. Clinical development was explored in a Phase I/II trial (NCT02332889), which was ultimately terminated.
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 autologous dendritic cell vaccine (University of Louisville).