Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The mRNA-electroporated dendritic cell product is an autologous, monocyte-derived dendritic cell (DC)-based cancer immunotherapy developed by Radboud University Medical Center. This therapeutic vaccine is produced by isolating monocytes from a patient, differentiating them into immature dendritic cells, and subsequently electroporating them with mRNA encoding the melanoma-associated antigens gp100 (melanocyte protein PMEL) and tyrosinase. The resulting antigen-loaded DCs are administered intranodally to the patient with the objective of priming and expanding tumor-specific CD4+ and CD8+ T-cell immune responses. It was primarily investigated for the treatment of high-risk uveal melanoma following local therapy, although clinical development was hindered by slow patient accrual in Phase 2 trials.
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 mRNA-electroporated dendritic cell product.