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PD-1 gene knocked out CD19/CD20/CD22/CD30-CART Treatment in Relapsed/Refractory CD19/CD20/ CD22/CD30+ Non Hodgkin Lymphoma

PD-1 gene knocked out CD19/CD20/CD22/CD30-CART Treatment in Relapsed/Refractory CD19/CD20/ CD22/CD30+ Non Hodgkin Lymphoma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800018713
Enrollment
Unknown
Registered
2018-10-05
Start date
2018-06-01
Completion date
Unknown
Last updated
2018-10-10

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

Conditions

Non Hodgkin Lymphoma

Interventions

Case series:Three days after cyclophosphamide and fludarabine chemotherapy, patients were treated with a dose of 1-10 x 106 CART positive T cells per kg body weight

Sponsors

Sun Yat-sen University Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Pathologic immunohistochemical or flow cytological examination confirmed CD19/CD20/CD22/CD30 positive malignant lymphoma; Previously received at least two lines of standard chemotherapy; Aged from 16 to 65 years; Estimated time of survival more than 3 months; ECOG=2; Vital organs function normally: cardiac ejection fraction =50%, normal ECG,CCr=40ml/min, ALT and AST =3 ULN, TBIL =2mg/dl, HGB =80g/L, Hgb=80g/L, ANC=1×109/L, PLT=50×109/L;Women of childbearing age with a negative pregnancy test; use contraception; with measurable lesions; Give signed informed consent before enrollment.

Exclusion criteria

Exclusion criteria: Used immunosuppressive drugs or glucocorticoids within 1 week before enrollment; Active infection; HIV test positive; Active hepatitis b or c infection; Pregnant or lactating women; Previous or combined history of other malignancies, not included: patients with cured basal or squamous cell carcinoma and in situ carcinoma of the cervix; participate in other clinical trials; Congenital immune deficiency; History of myocardial infarction and severe arrhythmia within 6 months; Uncontrolled hypertension, coronary heart disease, stroke, cirrhosis, nephritis and other serious complications.

Design outcomes

Primary

MeasureTime frame
Objective Response Rate;

Secondary

MeasureTime frame
complete response rate;Time to treatment failure;Progression-free survival time;overall survival;time to response;safety;

Countries

China

Contacts

Public ContactTongyu LIN

Sun Yat-sen University Cancer Center

tongyulin@hotmail.com+86 13926400320

Outcome results

None listed

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