Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Allogeneic CD19-STAR T cell is an investigational allogeneic T cell therapy developed for patients with relapsed or refractory (r/r) B-cell non-Hodgkin's lymphoma (B-NHL). This therapy involves synthetic T cell receptor (TCR) and antigen receptor (STAR) T cells, which are derived from healthy donors. The T cells are engineered using CRISPR-Cas9 gene editing to simultaneously knock out endogenous T cell receptor alpha constant (TRAC), human leukocyte antigen (HLA)-A/B, CIITA, and programmed death 1 (PD-1) genes. The STAR molecule is integrated into the TRAC locus. This strategic genetic modification aims to mitigate graft-versus-host-disease (GvHD) toxicity and host-versus-graft response, reduce the sensitivity of STAR T cells to immunosuppressive signals, and enhance their anti-tumor activity.
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 CD19-STAR T cell.