Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
gp100-TCR transduced CD8 T cells is an experimental adoptive cell therapy (ACT) consisting of CD8+ cytotoxic T lymphocytes genetically engineered to express a T-cell receptor (TCR) specific for the gp100 (glycoprotein 100) melanoma-associated antigen. The TCR is typically designed to recognize the gp100:280–288 epitope presented by HLA-A*0201 (HLA-A2) molecules on the surface of tumor cells. This therapy involves the ex vivo expansion and viral transduction (retroviral or lentiviral) of a patient's or donor's T cells before re-infusion. Once administered, these engineered cells target and eliminate gp100-expressing melanoma cells through MHC-restricted recognition. Research has been conducted primarily in academic settings, such as the National Cancer Institute (NCI), with some constructs provided by companies like Immunocore.
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 gp100-TCR transduced CD8 T cells.