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Enrolling by Invitation

NCT Number: NCT06616727

The Safety and Efficacy of SNC-109 CAR-T Cells Therapy the rGBM

A phase I study to evaluate the safety, tolerance and pharmacokinetics of SNC109 in patients with rGBM

Enrolling by Invitation

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Chinese PLA General Hospital

Beijing, China

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥18,both sexes;
  • Diagnosed with a history of glioblastoma, and the recurrent glioblastoma has confirmed by histological/molecular pathology (including astrocytoma World Health Organization (WHO) Grade 4);
  • Karnofsky (KPS) ≥50;
  • The estimated survival time is ≥12 weeks;
  • Blood pregnancy tests for women of childbearing age are negative;
  • The patient himself/herself, and/or his/her legal guardian, agree to participate in the trial and sign the informed consent form.

Exclusion criteria

  • Known allergies to study drugs or drugs that may be used in the study;
  • Severe concurrent diseases in the heart, lungs, liver, or other vital organs;
  • Hypertension is poorly controlled or accompanied by hypertensive crisis or hypertensive encephalopathy;
  • In addition to the glioblastoma, with other severe central nervous system diseases or complications or aggressive malignancies;
  • Long-term use of immunosuppressant drugs, or large doses of steroids;
  • Received live or attenuated vaccine or other surgery had no related to GBM within 4 weeks prior to Lymphocytes apheresis;
  • Lymphocytes apheresis or cell infusion combined with infection or unexplained fever.

Treatment and study plan

SNC109

Drug

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

Primary outcomes

  1. Incidence of treatment related adverse events

    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

  2. DLT

    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

Secondary outcomes

  1. Overall survival (OS) after infusion

    Time frame: within 2 years after first infusion

    The data of Overall survival (OS) after infusion

  2. Time maximum of SNC-109 Cell count and CAR vector copy number

    Time frame: within 2 years after first infusion

    Pharmacokinetic (PK) profile/parameter Tmax

  3. Pharmacokinetic (PK) profile/parameters Peak Plasma Concentration (Cmax) of SNC-109 Cell count and CAR vector copy number

    Time frame: within 2 years after first infusion

    Peak Plasma Concentration (Cmax)

  4. Pharmacokinetic (PK) profile/parameters Area under the plasma concentration versus time curve (AUC)

    Time frame: within 2 years after first infusion

    Area under the plasma concentration versus time curve (AUC) of SNC-109 Cell count

  5. Progression free survival (PFS) after infusion

    Time frame: within 2 years after first infusion

    The data of Overall survival (OS) after infusion

  6. Efficacy assesment for the treatment according to iRANO

    Time frame: within 2 years after first infusion

    Assessment of disease response rates according to the Immunological Response Assessment in Neuro-Oncology (iRANO)

  7. Pharmacodynamic (PD) profile/parameters Changes of Cytokines after infusion

    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

  8. Concentration of Human anti-chimeric antibody (HACA)

    Time frame: within 2 years after first infusion

    Detection of changes in peripheral blood and cerebrospinal fluid Human anti-chimeric antibody (HACA)

Sponsors and collaborators

Lead sponsor

Shanghai Simnova Biotechnology Co.,Ltd.

Industry

Registry information

Official study title

A Phase I Study to Evaluate the Safety, Tolerability and Pharmacokinetics of SNC109 in Patients With Recurrent Glioblastoma

Important dates

Study start
2023
Primary completion
2024
Study completion
2026
First posted
Sep 27, 2024
Registry last updated
Sep 27, 2024

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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