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A clinical study on the safety and effectiveness of chimeric antigen receptor modified T cells (CART) in the treatment of relapsed and refractory glioma

A clinical study on the safety and effectiveness of chimeric antigen receptor modified T cells (CART) in the treatment of relapsed and refractory glioma

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035410
Enrollment
Unknown
Registered
2020-08-10
Start date
2020-08-01
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

Glioma

Interventions

trial group:PMSA+GD2 CAR T

Sponsors

Guangdong Clifford Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) Grade IV glioma, with residual lesions or progression after surgery or radiotherapy, CT or MRI reveals that the maximum diameter of the residual tumor is >= 1cm; 2) Aged >=8 and = 80%; 6) ECOG =12 weeks; 8) Absolute lymphocyte value >= 0.8*10^9/L, ANC >= 0.75*10^9/L, PLT >= 75*10^9/L; 9) AST and AST do not exceed 5 times the upper limit of the normal value; 10) Bilirubin does not exceed 3 times the upper limit of normal; 11) Serum creatinine does not exceed 2 times the upper limit of normal; 12) The patient or family member signs an informed consent form.

Exclusion criteria

Exclusion criteria: 1) The disease progresses rapidly; 2) Receiving treatment with other new drugs and still in the care period; 3) Those who use immunosuppressive agents (including hormones); 4) History of severe heart and lung disease; 5) Actively infected persons (including viral and bacterial infections); 6) Those who suffer from other uncontrolled diseases that the researcher thinks are not suitable for joining; 7) CNS neuroblastoma patients with central nervous system involvement; 8) Any situation that the researcher believes may increase the risk of the subject or interfere with the test results.

Design outcomes

Primary

MeasureTime frame
Tumor size;PR, CR, SD, PD;

Secondary

MeasureTime frame
Behavioral Observation and Evaluation;Tumor markers;Survival time (survival rate);progression free time;Quality of life assessment;Toxic reaction (adverse reaction);

Countries

China

Contacts

Public ContactCai Qichun

Guangdong Clifford Hospital

purecai@163.com+86 13802830754

Outcome results

None listed

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