Clinical trials
Follow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This investigational cell therapy approach, developed by the Washington University School of Medicine, utilizes allogeneic hematopoietic stem cells in a sequential transplant strategy for patients with high-risk non-Hodgkin's lymphoma. The protocol involves an initial cytoreductive phase using high-dose chemotherapy followed by an autologous hematopoietic stem cell transplant. Approximately 60 to 120 days later, patients receive a non-myeloablative allogeneic hematopoietic stem cell transplant from HLA-identical related or unrelated donors. The allogeneic phase employs a conditioning regimen of total lymphoid irradiation (TLI) and anti-thymocyte globulin (ATG) to facilitate engraftment and induce a graft-versus-lymphoma (GVL) effect, where donor-derived immune cells target residual malignant cells, while minimizing the toxicities typically associated with myeloablative conditioning.
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 allogeneic hematopoietic stem cells (Washington University School of Medicine, 285e74).