Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
U2AF1Q157R neoantigen-specific TCR-T cells are a type of **adoptive cell therapy** in which a patient's own T cells are genetically engineered to express a T cell receptor (TCR) that specifically recognizes the mutant U2AF1 Q157R neoantigen, a tumor-specific mutation most commonly identified in myeloid malignancies such as myelodysplastic syndromes and acute myeloid leukemia. Upon reinfusion, these TCR-T cells can recognize and destroy cancer cells expressing the U2AF1 Q157R mutant peptide presented by human leukocyte antigen (HLA) molecules. The expected mechanism is highly targeted antitumor immunity, with a goal of eradicating malignant clones harboring the U2AF1 Q157R mutation while sparing normal tissue. This is a personalized cell therapy and is not a standardized small molecule or monoclonal antibody. The modality is cell therapy—specifically, T cell receptor engineered T cell therapy.
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 U2AF1Q157R neoantigen-specific TCR-T cells.