Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This personalized autologous dendritic cell vaccine was developed by the National Cancer Institute (NCI) for the treatment of pediatric solid tumors, specifically metastatic Ewing sarcoma and alveolar rhabdomyosarcoma. The therapy involves harvesting a patient's own dendritic cells and loading them ex vivo with synthetic peptides that represent the unique chromosomal translocation breakpoints characteristic of these tumors. For Ewing sarcoma, the vaccine typically targets the EWS-FLI1 or EWS-ERG fusion proteins, while for alveolar rhabdomyosarcoma, it targets PAX3-FOXO1 (PAX3-FKHR) or PAX7-FOXO1 (PAX7-FKHR). These pulsed dendritic cells are re-infused into the patient to act as professional antigen-presenting cells, priming and expanding tumor-specific cytotoxic T-lymphocytes. In clinical trial contexts, this vaccine has been evaluated following autologous T-cell transplantation and in combination with the protease inhibitor indinavir to enhance the anti-tumor immune response.
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 tumor antigen-pulsed dendritic cell vaccine (NCI).