ATLCAR.CD30.CCR4 cells
/ UNC Lineberger Comprehensive Cancer Center
- LARVOL DELTA
Home
Next
Prev
1 to 4
Of
4
Go to page
1
June 21, 2024
ATLCAR.CD30.CCR4 for CD30+ HL ATLCAR.CD30.CCR4 Cells
(clinicaltrials.gov)
- P1/2 | N=31 | Recruiting | Sponsor: UNC Lineberger Comprehensive Cancer Center | Not yet recruiting ➔ Recruiting
Enrollment open • IO biomarker • Hematological Malignancies • Hodgkin Lymphoma • Lymphoma • Oncology
October 19, 2023
ATLCAR.CD30.CCR4 for CD30+ HL ATLCAR.CD30.CCR4 Cells
(clinicaltrials.gov)
- P1/2 | N=31 | Not yet recruiting | Sponsor: UNC Lineberger Comprehensive Cancer Center
IO biomarker • New P1/2 trial • Hematological Malignancies • Hodgkin Lymphoma • Lymphoma • Oncology
December 03, 2021
CD30-Directed CAR-T Cells Co-Expressing CCR4 in Relapsed/Refractory Hodgkin Lymphoma and CD30+ Cutaneous T Cell Lymphoma
(TCT-ASTCT-CIBMTR 2022)
- "Pts are lymphodepleted with 3 days of bendamustine 70 mg/m 2 and fludarabine 30 mg/m 2...All pts had prior brentuximab vedotin and 11 pts had prior checkpoint inhibitors... CCR4.CD30.CAR-Ts are safe with promising efficacy even at the lowest DL in pts with r/r HL, suggesting that early tumor homing may improve antitumor activity. Our data serve as a proof of concept for future modifications of CAR-T cells to improve localization to tumor sites."
CAR T-Cell Therapy • IO biomarker • Bone Marrow Transplantation • Cutaneous T-cell Lymphoma • Hematological Malignancies • Hodgkin Lymphoma • Inflammation • Lymphoma • Oncology • T Cell Non-Hodgkin Lymphoma • Transplantation • CCR4 • TNFRSF8
November 05, 2021
CD30-Directed CAR-T Cells Co-Expressing CCR4 in Relapsed/Refractory Hodgkin Lymphoma and CD30+ Cutaneous T Cell Lymphoma
(ASH 2021)
- P1 | "All patients receive lymphodepletion with 3 days of bendamustine 70 mg/m 2 and fludarabine 30 mg/m 2...All patients had received prior brentuximab vedotin...Two patients had grade 2 cytokine release syndrome (CRS) which resolved with tocilizumab, and 1 had self-limiting grade 1 CRS...Interestingly, responses are already seen at the lowest dose level, suggesting that early tumor homing driven by CCR4 may allow more fitted cells to better exploit their antitumor potential. Our data serve as a proof of concept for future modifications of CAR-T cells to improve their localization to disease sites."
CAR T-Cell Therapy • IO biomarker • Bone Marrow Transplantation • Cutaneous T-cell Lymphoma • Hematological Malignancies • Hodgkin Lymphoma • Inflammation • Lymphoma • Oncology • T Cell Non-Hodgkin Lymphoma • Transplantation • CCR4 • TNFRSF8
1 to 4
Of
4
Go to page
1