Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
GT802 is an autologous chimeric antigen receptor (CAR) T-cell therapy targeting the CD19 antigen, currently under clinical investigation for the treatment of relapsing/refractory multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD). Developed by investigators at Tongji Hospital in collaboration with Wuhan Gene-Therapy Biopharmaceutical, GT802 is designed to deplete CD19-expressing B cells, which are key drivers of the inflammatory response and demyelination in these autoimmune central nervous system disorders. The therapy involves the genetic modification of a patient's own T cells to express a CAR that recognizes CD19, followed by re-infusion into the patient after lymphodepleting chemotherapy. Early clinical data suggest that GT802 may provide a potent and durable reduction in B-cell populations, potentially offering a new therapeutic option for patients who have not responded to conventional disease-modifying therapies.
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 GT802.