Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Autologous CD19 chimeric antigen receptor (CAR) T cells are an investigative cellular immunotherapy developed by Universitaetsklinikum Erlangen for the treatment of severe, steroid-refractory chronic graft-versus-host disease (cGvHD) and various systemic autoimmune diseases. The therapy involves the ex vivo genetic modification of a patient's own T cells using a lentiviral vector to express a second-generation CAR (typically featuring a 4-1BB costimulatory domain) that targets the CD19 antigen on B cells. Upon re-infusion, these engineered T cells mediate the systemic depletion of B cells, which are key drivers of the inflammatory and fibrotic processes in cGvHD and autoantibody production in diseases like systemic lupus erythematosus (SLE). This approach aims to achieve a "reset" of the immune system, potentially allowing for the re-establishment of immune tolerance and long-term drug-free remission.
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 autologous CD19 chimeric antigen receptor T cells.