RecruitingNot ApplicableNCT07144735

Allogeneic γδT Cells in Glioblastoma

Allogeneic Gamma Delta (γδ) T Cells for the Treatment of Glioblastoma

Sponsor

Peking University Third Hospital

Enrollment

18 participants

Start Date

Apr 1, 2025

Study Type

INTERVENTIONAL

Conditions

Glioblastoma Multiforme (GBM)Glioblastoma (GBM)

Summary

This first-in-human clinical study aims to evaluate the safety and feasibility of locally delivered, allogeneic γδ T cells (genetically edited with ARIH1 and BCL11b knockout, designated ABOUT γδT cells) in patients with glioblastoma multiforme (GBM). The engineered effector cells are delivered via localized administration to selectively target and eliminate residual GBM cells. ABOUT: ARIH1 and BCL11b knockOUT γδ T cells.

Eligibility

Min Age: 18 YearsMax Age: 70 Years

Inclusion Criteria21

Male or female, age 18-70 years old (both ends included)
At least one evaluable lesion with previous biopsy or pathohistologic confirmation of glioblastoma (WHO grade IV), with imaging suggestive of continued progression or recurrence after comprehensive treatment
Karnofsky Performance Status (KPS) ≥ 60%
Life expectancy \> 4 weeks
Patients who completed radiotherapy or systemic therapies (including temozolomide/bevacizumab or other agents) for at least 4 weeks prior to enrollment. All prior treatment-related toxicities should be defined as ≤ grade 1 (except for toxicities such as alopecia or leukoplakia) according to the Common Terminology Standard for Adverse Events (CTCAE 6.0)
Must be able to undergo an MRI with contrast
Must have adequate organ and marrow function as defined below:
White blood cell count (WBC) ≥ 3 x 10\^9/L
Absolute neutrophil count (ANC) \> 1 x 10\^9/L
Hemoglobin (Hb) ≥ 90 g/L
Platelet (PLT) ≥ 80×10\^9/L
Albumin transaminase (ALT) \& albumin transaminase (AST) \< 1.5 × institutional upper limit of normal (ULN)
Serum creatinine (Cr) \< 1.5 x institutional ULN
Total bilirubin \< 1.5 x institutional ULN
PT \& PTT ≤ 1.25 x institutional ULN
No obvious hereditary diseases
Normal cardiac function with left ventricular ejection fraction \>55%
No bleeding and coagulation disorders
Absence of positive blood cultures for bacteria, fungus, or virus within 48-hours prior to ABOUT γδT cell infusion and/or there aren't any indications of meningitis
Fertile women must have had a pregnancy test with a negative result within 7 days prior to the start of treatment, and subjects are willing to use contraception (hormonal or barrier method of birth control or abstinence) during the clinical trial and for 6 months after the last cell infusion; should a woman become pregnant or suspect that she is pregnant while participating on the trial, she should inform her treating physician immediately
Signed, written informed consent

Exclusion Criteria8

Active hepatitis B or C virus, HIV infection, or other untreated active infection
Pregnant and lactating women
Participants with organ failure
Participants with a chronic disease requiring immunologic or hormonal therapy
Participants with an allergy to immunotherapy and related cells
Participants with uncontrolled intercurrent illness
Participants with psychiatric illness/social situations that would limit compliance with study requirements
Participants with a history of organ transplantation or who are awaiting organ transplantation