New dual-targeting CAR t therapy tested for hard-to-treat lymphoma
NCT ID NCT05169489
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This early-phase study tested a new treatment called bbT369 for people with a type of blood cancer (B cell non-Hodgkin's lymphoma) that had come back or stopped responding to other treatments. The therapy uses a patient's own immune cells, which are modified to better recognize and attack cancer cells. The study aimed to check safety and how well the treatment works, but it was ended early.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
-
15 people
The number who actually took part.
- Started
-
Jan 2022
- Finished
-
Sep 2025
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * ≥18 years of age at the time of signing informed consent. * Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2. * Diagnosis of B-cell NHL according to WHO 2017 classification or WHO 2016 classification where applicable: 1. DLBCL (germinal center B cell \[GCB\] or activated B cell \[ABC\] type or not otherwise specified \[NOS\]) 2. HGBCL (with MYC and BCL2 and/or BCL6 rearrangements or NOS) 3. PMBCL 4. FL 3b 5. DLBCL transformed from FL * Participants must have relapsed or refractory (r/r) B cell NHL after autologous stem cell transplant (ASCT) or at least 2 prior lines of therapy including an anti-CD20 monoclonal antibody and an anthracycline containing chemotherapy regimen. Note: participants with DLBCL transformed from FL must have r/r disease after ASCT or at least 2 prior therapies following transformation irrespective of therapeutic agents. * At least 1 FDG-avid lesion per Lugano Classification criteria at time of enrollment. Exclusion Criteria: * Treatment with any investigational cellular therapy prior to enrollment. Treatment with an approved anti-CD19 CAR T cell therapy in an investigational setting may be permitted after discussion with and approval of the Sponsor. * Progression within 6 weeks of prior anti-CD19 CAR T cell therapy. * Residual toxicities or end-organ damage to vital organs from prior therapy that could put a subject at undue risk based on Investigator's assessment. Toxicities related to prior cytokine release syndrome (CRS) or neurotoxicity must be resolved. * If a subject has received prior anti-CD19 CAR T therapy, development of ≥ Grade 3 CAR T related CRS or ≥ Grade 3 neurotoxicity that in the opinion of the Investigator would cause unacceptable risk of toxicity to the subject upon treatment with bbT369. * Primary central nervous system (CNS) lymphoma or a history or presence of clinically relevant CNS pathology. * Active autoimmune disease requiring systemic immunosuppressive and/or cytotoxic therapy within the past two years. * Treatment with any prior anti-CD79a therapy. * Previous history of an allogeneic bone marrow transplantation. Autologous stem cell transplantation (ASCT) is permitted.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Diffuse large B cell lymphoma (DLBCL) are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Colorado Blood Cancer Institute
Denver, Colorado, 80218, United States
-
Moffitt Cancer Center
Tampa, Florida, 33612, United States
-
Sarah Cannon
Nashville, Tennessee, 37203, United States
-
Stanford Cancer Institute
Stanford, California, 94305, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Off-the-Shelf Gene-Edited immune cells tested against Hard-to-Treat lymphoma
- Proton beams vs. X-Rays: can a pricier radiation spare hearts and prevent second cancers?
- New antibody tested against aggressive blood cancer
- Can engineered immune cells beat tough B-Cell cancers?
- Can 'Memory-Enhanced' immune cells outsmart lymphoma?
- Can a Four-Drug cocktail outsmart resistant lymphoma?