Chinese PLA General Hospital
Beijing, China
NCT Number: NCT06616727
A phase I study to evaluate the safety, tolerance and pharmacokinetics of SNC109 in patients with rGBM
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 1
Beijing, China
It is planned to recruit about 50 patients with rGBM subjects. The protocol consists of screening period, Lymphocytes apheresis period, Operation period, pre-infusion evaluation (-2~-1 days), infusion (day 0), infusion observation (day 1-post infusion), and follow-up period (last infusion-720 days). The incidence of dose limitation toxicity (DLT) will be observed within 28 days after the first infusion. Subjects in this study will receive multiple infusions, starting with 5×104 CAR+ T cells/dose in the first subject, and the Safety Review Committee (SRC) will evaluate the subsequent dosing regimen, dose, infusion interval, and number of treatment cycles. Subsequent subjects will be evaluated by the SRC on the basis of available PK and safety data, and the SRC will determine the dosing regimen, dose, infusion interval and number of treatment cycles based on observed evidences.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
SNC-109 CAR-T Cells, first dose from 5×104 CAR+ T Cells, treatment follows the operation and the next dose would be deiced by SRC
Time frame: Up to 28 days after first infusion
Incidence of adverse events associated with CAR-T cell transfusion within 28 days of the first infusion, abnormal and clinical significant laboratory results
Time frame: Up to 28 days after first infusion
Incidence of DLT associated with CAR-T cell transfusion within 28 days of the first infusion
Time frame: within 2 years after first infusion
The data of Overall survival (OS) after infusion
Time frame: within 2 years after first infusion
Pharmacokinetic (PK) profile/parameter Tmax
Time frame: within 2 years after first infusion
Peak Plasma Concentration (Cmax)
Time frame: within 2 years after first infusion
Area under the plasma concentration versus time curve (AUC) of SNC-109 Cell count
Time frame: within 2 years after first infusion
The data of Overall survival (OS) after infusion
Time frame: within 2 years after first infusion
Assessment of disease response rates according to the Immunological Response Assessment in Neuro-Oncology (iRANO)
Time frame: within 2 years after first infusion
Changes of cytokines (such as Interleukin-6, Interleukin-8 etc.) in peripheral blood (PB) and cerebrospinal fluid (CSF) pre-and post- infusion and at each of the main follow-up time points, and the time to recovery
Time frame: within 2 years after first infusion
Detection of changes in peripheral blood and cerebrospinal fluid Human anti-chimeric antibody (HACA)
Shanghai Simnova Biotechnology Co.,Ltd.
Industry
A Phase I Study to Evaluate the Safety, Tolerability and Pharmacokinetics of SNC109 in Patients With Recurrent Glioblastoma
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.
Published trials that share one or more normalized conditions with this study.
NCT03914768
Astrocytoma, Brain Diseases
Shenzhen, Guangdong, China
View Trial DetailsNCT07634575
Astrocytoma, Glioblastoma
London, United Kingdom
View Trial DetailsNCT07417774
Astrocytoma, Glioblastoma
Tucson, Arizona, United States
View Trial DetailsNCT07130149
Astrocytoma, Glioblastoma
Zhengzhou, Henan, China
View Trial Details