Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This therapeutic regimen is a combination of a donor-derived dendritic cell (DC) vaccine and donor lymphocyte infusion (DLI) developed by the National Cancer Institute (NCI). It is specifically designed for patients with WT1-expressing hematologic malignancies—including acute myeloid leukemia (AML), acute lymphocytic leukemia (ALL), chronic myeloid leukemia (CML), myelodysplastic syndromes (MDS), and lymphomas—who have relapsed after allogeneic hematopoietic stem cell transplantation. The vaccine consists of monocyte-derived dendritic cells pulsed with three HLA-A2 binding Wilms' tumor 1 (WT1) peptides (WT1 37–45, 126–134, and 187–195) linked to an HIV TAT protein transduction domain. The goal of the vaccine is to stimulate a donor-derived, WT1-specific T-cell response, which is further augmented by the infusion of donor lymphocytes to enhance the graft-versus-leukemia (GVL) effect.
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 WT1 peptide-loaded allogeneic dendritic cell vaccine + donor lymphocyte infusion.