Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
ESO-T01 is a third-generation, non-replicative, self-inactivating lentiviral vector designed to deliver a BCMA-targeted chimeric antigen receptor (CAR) gene directly into patients’ T cells in vivo. Unlike traditional ex vivo CAR-T therapies, ESO-T01 is administered as an “off-the-shelf” single intravenous dose that reprograms the patient’s own T cells within their body to express the anti-BCMA CAR. This approach eliminates the need for lymphodepletion and complex cell manufacturing processes. The therapy leverages EsoBiotec’s ENaBL platform technology to achieve immune-shielded delivery and robust in vivo transduction of T cells. ESO-T01 is being developed primarily for relapsed/refractory multiple myeloma and has shown promising early safety and efficacy signals in phase 1 clinical trials, with potential expansion into autoimmune diseases.
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 ESO-T01.