The goal of this clinical trial is to estimate the safety, tolerance and initial efficacy of target IL-13Rα2 or B7-H3 UCAR-T cell injection in the treatment of patients with advanced glioma, as well as the pharmacokinetic characteristics of its metabolites after single and multiple administrations and the biomarkers related to efficacy, safety and drug metabolism.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
12
local administration (intracranial cavity or intravertebral injection after surgery): 1 ampoule (about 2-5 ml, 1-5×10\^7 cells) for 1-2 minutes each time.
local administration (intracranial cavity or intravertebral injection after surgery): 1 ampoule (about 2-5 ml, 1-5×10\^7 cells) for 1-2 minutes each time.
The Second Affiliated Hospital of Soochow University
Suzhou, Jiangsu, China
RECRUITINGObjective Response Rate
The proportion of patients whose tumor size decreases to the expected value and can continue to meet the expected minimum time limit。
Time frame: Up to 5 years or complete the follow-up of the last enrolled patient, whichever comes first.
Progression-Free Survival
The time from enrolling into the trial to the first occurrence of disease progression or death from any cause。
Time frame: Up to 5 years or complete the follow-up of the last enrolled patient, whichever comes first.
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