Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This experimental autologous cellular immunotherapy, developed by Duke University, is designed for the treatment of metastatic melanoma. The vaccine is produced by harvesting a patient's own monocytes via leukapheresis and differentiating them into mature dendritic cells (DCs). These DCs are then transfected via electroporation with messenger RNA (mRNA) encoding tumor-associated melanoma antigens. In specific clinical protocols, a subset of these DCs is also transfected with mRNA encoding immune-modulatory proteins, such as GITR ligand (GITR-L) and a monoclonal antibody against CTLA-4. This approach aims to deliver immune modulators locally at the site of vaccination (typically the lymph nodes) to enhance the activation and expansion of tumor-specific T cells while avoiding the systemic toxicities associated with intravenous administration of checkpoint inhibitors. The vaccine is administered via ultrasound-guided intranodal injection.
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 RNA-transfected autologous dendritic cell vaccine (Duke University).