Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This experimental cellular immunotherapy is a vaccine composed of donor-derived dendritic cells (DCs) designed to enhance the graft-versus-leukemia (GVL) effect following allogeneic hematopoietic stem cell transplantation (HSCT). The vaccine cells are ex vivo loaded with minor histocompatibility antigens (MiHAs), which are polymorphic peptides that differ between donor and recipient and are specifically expressed on the patient's malignant cells. To prevent T-cell exhaustion and inhibition through the PD-1 pathway, the dendritic cells are genetically modified using small interfering RNA (siRNA) to silence the expression of programmed death-ligand 1 (PD-L1) and programmed death-ligand 2 (PD-L2). By presenting MiHAs in the absence of these inhibitory signals, the vaccine aims to prime and expand MiHA-specific donor T cells, promoting the targeted elimination of residual leukemic cells. This therapeutic approach was primarily developed by the Radboud University Medical Center for use in patients with high-risk hematological malignancies.
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 minor histocompatibility antigen-loaded programmed death-ligand 1 and programmed death-ligand 2-silenced donor dendritic cell vaccine.