Dushu Lake Hospital Affiliated to Soochow University
Suzhou, Jiangsu, 215125, China
Location status: Recruiting
Location contact
Xuetao Li
CONTACT
Xuetao Li
SUB_INVESTIGATOR
Yulun Huang
CONTACT
Yulun Huang
PRINCIPAL_INVESTIGATOR
NCT Number: NCT06018363
B7-H3 is expressed at low levels in normal tissues but overexpressed in various tumor tissues. The ubiquitous expression of B7-H3 in tumors of different grades is a key feature for brain gliomas. The immunohistochemistry study showed that B7-H3 is abundantly expressed on both glioma (especially high-grade glioma) cells and tumor-associated endothelial cells. For GBM, the expression of B7-H3 is intensely positive, especially on tumor cells and vascular endothelial cells, which makes B7-H3 a potential immunotherapeutic target.
γδ T cells recognize tumor cells without being restricted by MHC molecules, and thus can be used in allogeneic therapy without the risk of causing graft-versus-host disease.
This study is an open-label, single-arm, dose-escalation and dose-expansion clinical study aimed at evaluating the safety and efficacy of allogeneic B7-H3 CAR γδT in patients with malignant glioma.
Interested in participating?
Request Info18 year–70 year
All sexes
Interventional
Phase 1 / Phase 2
Suzhou, Jiangsu, 215125, China
Location status: Recruiting
Xuetao Li
CONTACT
Xuetao Li
SUB_INVESTIGATOR
Yulun Huang
CONTACT
Yulun Huang
PRINCIPAL_INVESTIGATOR
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Dose escalation (3+3) : dose 1 (1 × 10^7 CAR+cells) , dose 2 (3 × 10^7 CAR+cells), dose 3 (6× 10^7 CAR+cells), once every 4 weeks via an Ommaya reservoir or intrathecal administration.
Dose expansion 1: dose of RP2D, once every 4 weeks via an Ommaya reservoir or intrathecal administration.
Dose expansion 2: 3 × 10^7 CAR+cells, every two weeks for three consecutive months, then changed to once every 4 weeks via an Ommaya reservoir or intrathecal administration.
Time frame: 12 months
AE is defined as any adverse medical event from the date of the cell infusion to 12 months after B7-H3 CAR-γδT cells infusion. Among them, cytokine release syndrome (CRS) and immune cell-associated neurotoxicity syndrome (ICANS) were graded according to American Society for Transplantation and Cellular Therapy (ASTCT) criteria, graft-versus-host disease (GVHD) according to criteria defined by the Mount Sinai Acute GVHD International Consortium. Other AEs were graded according to common terminology criteria for adverse events (CTCAE) v5.0.
Time frame: 28 days after the first dose of B7-H3 CAR-γδT cells
DLT was defined as B7-H3 CAR-γδT cells-related events with onset within first 28 days following infusion
Time frame: 28 days after the first dose of B7-H3 CAR-γδT cells
Time frame: 28 days after the first dose of B7-H3 CAR-γδT cells
Time frame: 28 days after the first dose of B7-H3 CAR-γδT cells
Time frame: 28 days after the first dose of B7-H3 CAR-γδT cells
Time frame: 6 months, 9 months and 12 months
Time frame: 6 months
Time frame: 6 months
Dushu Lake Hospital Affiliated to Soochow University
Other
Allogeneic B7-H3 CAR-γδT Cell Therapy Recurrent/Progressive High Grade Glioma(R/R HGG)
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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