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CD22 CAR T–cell therapy for relapse or refractory B-cell Lymphoma or acute B lymphocytic leukemia

CD22 CAR T–cell therapy for relapse or refractory B-cell Lymphoma or acute B lymphocytic leukemia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800019298
Enrollment
Unknown
Registered
2018-11-04
Start date
2018-11-01
Completion date
Unknown
Last updated
2018-11-19

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

Conditions

Relapse or refractory B-cell Lymphoma or acute B lymphocytic leukemia

Interventions

CD22 CAR-T after CD19 CAR-T treatment failure group:CD22 CAR-T treatment
CD22 CAR-T combination with CD19 CAR-T treatment group:CD22 CAR-T combination with CD19 CAR-T treatment

Sponsors

Tianjin First Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. The patient or his/her legal guardians must sign a consent form; 2. The patient ages 12 years to 80 years, a male or female; 3. The patient was diagnosed as relapse or refractory B-cell Lymphoma or acute B lymphocytic leukemia by pathology, histology and flow cytometry; 4. main organs seem to be functioning well: Liver function: bilirubin=34.2umol/L; Renal function: Serum creatinine<220umol/L; Lung function: arterial oxygen saturation=95%; Heart function: LVEF=40%; 5. peripheral venous blood in patients flow smoothly; 6. Karnofsky score=60.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. Patients who want to be pregnant in 1 year; 3. Patients who can not use contraception in 1 year; 4. Uncontrolled active infection with in 4 weeks; 5. Active hepatitis B or hepatitis C virus infection; 6. HIV infected patients; 7. The patients with other cancers diagnosised by pathology; 8. Patients with serious autoimmune diseases or immunodeficiency; 9. Patients who suffer from allergies; 10. Patients who have taken part in other clinical tests within 6 weeks; 11. Patients who use systemic steroids before treatment within 4 weeks; 12. Patients who have a history of central nervous system disease; 13. Patients who are addicted to some drugs; 14. Patients who are not allowed to take part in the test(judged by the researchers).

Design outcomes

Primary

MeasureTime frame
remission rate;

Secondary

MeasureTime frame
Progression-free survival;Overall survival;

Contacts

Public ContactDeng Qi

Tianjin First Central Hospital

kachydeng@hotmail.com+86 13612055872

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026