Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
ET019002-T is an **autologous T cell therapy** genetically engineered to express a novel anti-CD19 chimeric antigen receptor (CAR) for the treatment of **relapsed/refractory B-cell malignancies**. Developed using the ARTEMIS platform by Eureka Therapeutics, these T cells are transduced via lentivirus with an anti-CD19 single-chain variable fragment (scFv) fused to CD28, granting targeted antitumor effects against CD19+ cells. ET019002-T demonstrates similar efficacy to classical CAR-T cells in preclinical studies with significantly lower inflammatory cytokine release, aimed at improving safety in clinical use. Clinical administration is performed via intravenous infusion, following pre-conditioning with cytotoxic agents when appropriate. Early clinical trials report safety and preliminary efficacy, including cases of complete remission in advanced disease[1][2][4][6][8][9][10].
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 ET019002-T.