Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Autologous anti-MART-1 F5 T-cell receptor gene-engineered peripheral blood lymphocytes are a personalized cell therapy product created by isolating a patient’s own (autologous) peripheral blood mononuclear cells (PBMCs), genetically engineering them ex vivo with a retroviral vector to express the high-affinity DMF5-derived, HLA-A2-restricted, anti-MART‑1 (Melan-A) specific α/β T cell receptor, and expanding them for reinfusion. Upon administration, these engineered cytotoxic CD8+ and CD4+ lymphocytes specifically recognize and target melanoma cells expressing the MART‑1 antigen in the context of HLA-A*0201. The therapy is typically combined with preparative chemotherapy for host immune depletion, dendritic cell vaccination pulsed with MART‑126–35 peptide to boost in vivo expansion of transferred cells, and low-dose interleukin 2 to support persistence. This approach aims to induce tumor regression in patients with metastatic melanoma refractory to standard treatments[2][3][6].
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 anti-MART-1 F5 T-cell receptor gene-engineered peripheral blood lymphocytes.