Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CD19-zeta transduced Epstein-Barr virus-specific cytotoxic T lymphocytes represent a specialized form of chimeric antigen receptor (CAR) T-cell therapy pioneered by the Center for Cell and Gene Therapy at Baylor College of Medicine. These cells are T-lymphocytes with native specificity for Epstein-Barr Virus (EBV) antigens that have been genetically modified to express a first-generation CAR targeting the CD19 protein found on B-cells. The construct typically consists of a CD19-specific single-chain variable fragment (scFv) linked to a CD3-zeta signaling domain without additional costimulatory domains (such as CD28 or 4-1BB). This dual-specific approach leverages the EBV-specific T-cell receptor (TCR) to allow the cells to receive physiological survival and proliferation signals from endogenous EBV-infected cells or latent EBV in the host. This mechanism is designed to enhance the persistence and anti-tumor activity of the CAR-T cells compared to standard CAR-T cells that lack such native viral specificity. The therapy has been primarily investigated for the treatment of CD19-positive B-cell malignancies, including B-cell lymphoma and chronic lymphocytic leukemia.
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 CD19-zeta transduced Epstein-Barr virus-specific cytotoxic T lymphocytes.