Skip to content

Biology understanding of CD19 CAR-T cell therapy and the preclinical exploration of CAR-T cell therapy plus immune checkpoint inhibitors combination in large B-cell lymphoma

Biology understanding of CD19 CAR-T cell therapy and the preclinical exploration of CAR-T cell therapy plus immune checkpoint inhibitors combination in large B-cell lymphoma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400088705
Enrollment
Unknown
Registered
2024-08-26
Start date
2024-11-21
Completion date
Unknown
Last updated
2026-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Large B-cell lymphoma

Interventions

Prospective samples collection group:NA
Retrospective data collection group:NA

Sponsors

Beijing GoBroad Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Histologically confirmed large B-cell lymphoma, including diffuse large B-cell lymphoma, or diffuse large B-cell lymphoma with secondary central nervous system involvement, or transformed follicular lymphoma, or primary mediastinal large B-cell lymphoma, or primary mediastinal large B-cell lymphoma with CNS involvement, or high-grade B-cell lymphoma with MYC and BCL2 or BCL6 translocation; 2. Relapsed or refractory patients, defined as those who failed to achieve complete response (CR) or relapsed early after standard immunochemotherapy (such as R-CHOP or similar therapies); 3. Evaluable lesions (Lugano 2014 as evaluation criteria); 4. For the portion that residual tumor tissue samples and residual CD19 CAR T cell products need to be collected, patients are required to sign the Informed Consent Form(ICF) and are available to provide at least one of the two options: the remaining tumor tissue or the residual CAR T cell products.

Exclusion criteria

Exclusion criteria: 1. Other diagnosis of non-Hodgkin lymphoma besides inclusion criteria; 2. Patients who have used other CART cell therapy or other gene-modified cell therapy before first receiving CD19 CART cell.

Design outcomes

Primary

MeasureTime frame
CAR-T product exhaustion status;dynamic change in CAR T copy number;dynamic change in CAR T cells in peripheral blood;dynamic change in subclusters of CAR T cells and their checkpoints expression in peripheral blood;tumor CD19 expression;dynamic change of tumor microenvironment post-CAR T infusion;tumor infiltrating endogenous T cell subcluster and exhaustion status;CAR-T product exhaustion status;

Secondary

MeasureTime frame
CAR-T product subclusters;

Countries

China

Contacts

Public ContactKai Hu

Beijing GoBroad Hospital

huk@borenhospital.com+86 15010390336

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026