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Improving killing of renal cell carcinoma through the combined effects of TCR engineered CD4+ and CD8+ T cells (Section 39) - Mar 5, 2024 - Abstract #AACR2024AACR_5067; P1 In conclusion, these data show that CD4+ BZ-4 T cells transfected with the CD8 co-receptor acquire the ability to lyse RCC tumors at levels comparable to that observed in CD8+ BZ-4 T cells. Additional experiments are planned to evaluate whether mixtures of CD8+ BZ-4 T cells with CD4+ BZ-4-8 T cells will augment the ability of TCR modified T cells to proliferate in vivo and kill human RCC tumors compared to CD8+ BZ-4 T cells alone in tumor bearing NSG mice.
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Enrollment closed, Enrollment change, Trial primary completion date, Metastases: HERV-E TCR Transduced Autologous T Cells in People With Metastatic Clear Cell Renal Cell Carcinoma (clinicaltrials.gov) - Nov 13, 2023 P1, N=16, Active, not recruiting, Our initial results support the further development of HERV-E-directed therapies that focus on methods to improve in vivo persistence of TCR engineered T-cells and to target HERV-E antigens expressed on more commonly expressed HLA alleles. Recruiting --> Active, not recruiting | N=24 --> 16 | Trial primary completion date: Apr 2024 --> Oct 2023
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Trial completion date, Trial primary completion date, Metastases: HERV-E TCR Transduced Autologous T Cells in People With Metastatic Clear Cell Renal Cell Carcinoma (clinicaltrials.gov) - Sep 10, 2022 P1, N=24, Recruiting, For pts in DL4, HERV-E TCR were observed to proliferate in vivo, traffic to a metastatic site, and induce tumor regression in one mccRCC pts. Trial completion date: Dec 2022 --> Dec 2032 | Trial primary completion date: Dec 2022 --> Apr 2024
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