Drug intelligence / Profile preview

Allogeneic CD19-STAR T cell

Development stage
Phase 2
Lead developer
BriSTAR Immunotech
Modality
CRISPR-Cas9 → CRISPR Systems → Programmable Nucleases → Gene Editing → Gene Therapies, TCR-Engineered T Cells → Engineered T Cells → Adoptive Cell Transfer → Cell Therapies
Administration
Intravenous
01

Overview

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.

Other names
Allogeneic CD19-targeting STAR T cellsAllogeneic TRAC Locus-inserted CD19-targeting Synthetic T-cell Receptor Antigen Receptor (STAR) T Cells
02

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