Trial | NCT03880279  Report issue

Title

Autologous TAC T Cells Targeting CD19 in R/R Large B-Cell Lymphoma
A Phase I/II Trial Investigating Safety and Efficacy of Autologous TAC T Cells Targeting CD19 in Relapsed or Refractory Large B-Cell Lymphoma

  • Phase

    Phase 1/Phase 2

  • Study Type

    Interventional

  • Status

    Withdrawn

  • Study Participants

    0
Phase I/II study to evaluate TAC01-CD19 in subjects with relapsed or refractory B-cell lymphomas. TAC technology is a novel way to genetically modify T cells and to redirect these T cells to target cancer antigens by co-opting the natural T cell receptor. The dose finding portion of this study will evaluate the safety and tolerability of increasing dose levels of TAC01-CD19 to identify a Maximal Tolerated Dose (MTD) or Recommended Phase II Dose (RP2D). The dose expansion portion of the study will further evaluate the safety, efficacy and pharmacokinetics of TAC01-CD19 at the RP2D.
Study Started
May 31
2020
Anticipated
Primary Completion
Apr 30
2022
Anticipated
Study Completion
Apr 30
2024
Anticipated
Last Update
Feb 23
2022

Biological TAC01-CD19

Dose-escalating cohorts plus expansion groups

TAC01-CD19 Experimental

TAC01-CD19, Autologous TAC (T cell antigen coupler) T cells, single infusion, multiple dosage levels.

Criteria 

Inclusion Criteria:

Histologically confirmed CD19+ Large B-Cell Lymphoma including Diffuse Large B-cell Lymphoma (DLBCL) not otherwise specified (including de novo and transformed lymphoma), Primary Mediastinal Large B-cell Lymphoma, High-Grade B-cell Lymphoma with MYC and BCL2 and/or BCL6 rearrangement per WHO 2016 classification.
Relapsed or refractory disease after greater than 2 lines of therapy including anthracycline and anti-CD20 therapy and either having failed autologous stem cell transplant (ASCT) or being ineligible for ASCT.
ECOG 0-1.
Adequate organ function.

Exclusion Criteria:

Prior treatment with any of the following: allogeneic bone marrow transplantation, gene therapy, adoptive cell transfer of any kind, including CAR T cells.
Active central nervous system (CNS) lymphoma involvement.
History or presence of clinically relevant CNS pathology.
Active inflammatory neurological disorders, autoimmune disease, or infections.
No Results Posted