Inventor of the ImmTAC soluble TCR bispecific; tebentafusp was the first to improve survival in a solid tumour.
Immunocore, based in Abingdon and listed as IMCR, invented the ImmTAC soluble T-cell receptor bispecific, and its tebentafusp was the first drug of the format to improve survival in a solid tumour. Tebentafusp, sold as Kimmtrak, was proved in IMCgp100-202 in uveal melanoma; brenetafusp targets PRAME and is in the PRISM-MEL-301 phase 3 in melanoma; and IMC-R117C targets PIWIL1 in colorectal cancer. OnCo links it to melanoma and uveal melanoma, to PRAME as a target, to Oxford Cancer, and to the idea of antibodies that recognise mutant KRAS and p53 fragments displayed on the cell surface. Whether soluble TCR bispecifics can work in common solid tumours beyond uveal melanoma is the open question. Tebentafusp has its own page.
The first drug to improve survival in metastatic uveal melanoma, and the first TCR-based bispecific.
Brenetafusp is a soluble T-cell receptor bispecific, tebentafusp's successor, that recognises a PRAME peptide on HLA-A*02:01 and drags T cells onto the tumour. A phase 3 with nivolumab in first-line melanoma is enrolling, but only patients carrying HLA-A*02:01, about half of those of European ancestry, are eligible.
Shares IMCgp100-202, Tebentafusp, Oxford Cancer (Oxford University Hospitals and University of Oxford), Uveal melanoma.
Shares IMCgp100-202, Tebentafusp, Uveal melanoma, Melanoma.
Shares Brenetafusp, PRAME, Tebentafusp, Uveal melanoma.
Shares IMCgp100-202, Tebentafusp, Uveal melanoma, Melanoma.
Shares Brenetafusp, PRAME, Tebentafusp, Uveal melanoma.
Shares Brenetafusp, PRAME, Tebentafusp, Melanoma.
Shares Brenetafusp, PRAME, Tebentafusp, Uveal melanoma.
Shares Antibodies that see mutant KRAS and p53 fragments displayed on the cell surface, PRAME, Melanoma.