Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
T-allo10 is an investigational cell therapy product composed of donor-derived allogeneic CD4+ T cells enriched for type 1 regulatory T (Tr1) cells. These are generated ex vivo by coculturing donor CD4+ T cells with tolerogenic dendritic cells (DC-10s) for 10 days, resulting in a population that is specific for host alloantigens and capable of suppressing host-reactive immune responses. The primary mechanism involves suppression of graft-versus-host disease (GvHD) after hematopoietic stem cell transplantation (HSCT), while supporting immune reconstitution. Tr1 cells mediate their effects through high expression of CTLA-4 and PD-1, as well as secretion of IL-10, leading to targeted immunosuppression without global immune compromise. The therapy aims to reduce the incidence and severity of GvHD in patients receiving mismatched related or unrelated donor HSCT for hematologic malignancies such as acute lymphoblastic leukemia. Clinical trials have demonstrated safety and promising efficacy in pediatric and young adult populations[2][3][5][7][9].
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 T-allo10.