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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04406610
Other study ID # CAR-T
Secondary ID
Status Withdrawn
Phase Phase 1/Phase 2
First received
Last updated
Start date September 1, 2015
Est. completion date October 15, 2016

Study information

Verified date July 2020
Source Fuda Cancer Hospital, Guangzhou
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the safety and effectiveness of CAR-T cell immunotherapy in treating with GD2 positive glioma patients.


Description:

Chimeric antigen receptor (CAR) is a recombinant receptor with both antigen-binding and T cell activating functions. Chimeric antigen receptor T cell Immunotherapy has more advantages compared with conventional immunotherapy, especially in dealing with patients of hematologic malignancies and solid malignant tumors.This study design a novel specific Chimeric antigen receptor aiming at GD2 antigen.After CAR-T cell infusion,At periodic intervals, the investigators will evaluate clinical symptoms Improved conditions of this disease.Through this study,the investigators will evaluate the safty and effectiveness of CAR-T cell immunotherapy in treating with GD2 positive glioma patients.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date October 15, 2016
Est. primary completion date August 15, 2016
Accepts healthy volunteers No
Gender All
Age group 30 Years to 70 Years
Eligibility Inclusion Criteria:

- All standard therapies have failed according to NCCN guidelines or the patient refuses standard therapies after cancer recurrence

- Body tumor 1-6, the maximum tumor length < 2 cm

- KPS = 70, lifespan > 6 months

- Platelet count = 80×109/L,white blood cell count = 3×109/L, neutrophil count = 2×109/L, hemoglobin = 80 g/L

Exclusion Criteria:

- Patients with cardiac pacemaker

- Patients with brain metastasis

- Patients with grade 3 hypertension or diabetic complication, severe cardiac and pulmonary dysfunction

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
GD2 CAR-T immunotherapy
Antigen-specific T cell therapy

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Fuda Cancer Hospital, Guangzhou

Outcome

Type Measure Description Time frame Safety issue
Primary Classification of adverse reactions To observe the common 1-4 levels of side effects 3 months
Secondary Progression free survival (PFS)of patients PFS was defined as the interval between treatment initiation and local relapse, distant metastasis, or death, whichever occurred first. 1 year
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