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Different B cell target CART cells for sequential treatment of relapsed and refractory adult invasive B cell lymphoma

Different B cell target CART cells for sequential treatment of relapsed and refractory adult invasive B cell lymphoma

Status
Recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900020980
Enrollment
Unknown
Registered
2019-01-23
Start date
2019-01-23
Completion date
Unknown
Last updated
2019-01-28

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

Conditions

relapsed and refractory adult invasive B cell lymphoma

Interventions

Case series:CART cell sequential treatment

Sponsors

Beijing Boren Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Confirmation of a recurrent refractory invasive B-cell lymphoma with a positive target marker (a lymphoma cell expressing a therapeutic target antigen such as CD19, CD22, CD20) (standard reference NCCN guidelines, 5th edition, 2017); Recurrent invasive B-cell lymphoma refers to patients with invasive B-cell lymphoma who have re-emerged with increased tumor burden after CR, and refractory invasive B-cell lymphoma refers to invasive B cells that have not reached CR after 4 cycles of standard chemotherapy. Lymphoma patients. 2. Patients must have evaluable disease certificates, including minimal residual disease; 3. Aged 18-70 years old; 4. Estimated survival period of more than 3 months; 5. ECOG score 0-2 points; 6. Women of childbearing age are negative for the blood pregnancy test before the start of the trial and agree to take effective contraceptive measures during the trial period until the last follow-up.

Exclusion criteria

Exclusion criteria: 1. Primary central nervous system invasive B-cell lymphoma or invasive B-cell lymphoma involving the central nervous system; 2. History of epilepsy or other central nervous system disorders; 3. Active hepatitis B or hepatitis C virus infection, HIV, cytomegalovirus, EB virus infection or other unhealed active infections; 4. Pregnant or lactating women; 5. Those who have used any gene therapy product before; 6. Any situation that the investigator believes may increase the risk of the subject or interfere with the results of the test.

Design outcomes

Primary

MeasureTime frame
safety;

Secondary

MeasureTime frame
Ratio of bone marrow and peripheral B leukemia cells;

Countries

China

Contacts

Public ContactXiaoyan Ke

Beijing Boren Hospital

dongq@borenhospital.com+86 010-632900606

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 8, 2026