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SNPMiner SNPMiner Trials (Home Page)


Report for Mutation C18S

Developed by Shray Alag, 2020-2021.
SNP Clinical Trial Gene

There is one clinical trial.

Clinical Trials


1 A Phase 1, Open-Label Study Evaluating the Safety, Tolerability and Efficacy of LCAR-C18S, an CAR-T Cell Therapy Targeting Claudin18.2 in Patients With Advanced Gastric Cancer

This is a prospective, single-arm, single-center, open-label, single-dose Phase 1 dose finding and extension study to evaluate the safety, tolerability, pharmacokinetics, and anti-tumor efficacy profiles of the cell-based LCAR-C18S (hereinafter "LCAR-C18S") in subjects with Claudin18.2-positive advanced gastric adenocarcinoma.

NCT04467853
Conditions
  1. Gastric Cancer
Interventions
  1. Biological: LCAR-C18S cells
MeSH:Stomach Neoplasms
HPO:Neoplasm of the stomach

A Phase 1, Open-Label Study Evaluating the Safety, Tolerability and Efficacy of LCAR-C18S, an CAR-T Cell Therapy Targeting Claudin18.2 in Patients With Advanced Gastric Cancer. --- C18S ---

A Clinical Study to Evaluate CAR-T Cell-based Medicinal Product in the Treatment of Advanced Gastric Cancer This is a prospective, single-arm, single-center, open-label, single-dose Phase 1 dose finding and extension study to evaluate the safety, tolerability, pharmacokinetics, and anti-tumor efficacy profiles of the cell-based LCAR-C18S (hereinafter "LCAR-C18S") in subjects with Claudin18.2-positive --- C18S ---

A Clinical Study to Evaluate CAR-T Cell-based Medicinal Product in the Treatment of Advanced Gastric Cancer This is a prospective, single-arm, single-center, open-label, single-dose Phase 1 dose finding and extension study to evaluate the safety, tolerability, pharmacokinetics, and anti-tumor efficacy profiles of the cell-based LCAR-C18S (hereinafter "LCAR-C18S") in subjects with Claudin18.2-positive --- C18S --- --- C18S ---

Incidence of anti-LCAR-C18S antibody and positive sample titer. --- C18S ---

Venous blood samples will be collected to measure LCAR-C18S positive cell concentrations and the transgenic level of LCAR-C18S, at the time points when anti-LCAR-C18S antibody serum samples are evaluated. --- C18S ---

Venous blood samples will be collected to measure LCAR-C18S positive cell concentrations and the transgenic level of LCAR-C18S, at the time points when anti-LCAR-C18S antibody serum samples are evaluated. --- C18S --- --- C18S ---

Venous blood samples will be collected to measure LCAR-C18S positive cell concentrations and the transgenic level of LCAR-C18S, at the time points when anti-LCAR-C18S antibody serum samples are evaluated. --- C18S --- --- C18S --- --- C18S ---

Objective Response Rate (ORR) is defined as the proportion of subjects who achieve CR or PR after treatment via LCAR-C18S cell infusion, and the objective tumor response rate will be calculated for patients with measurable disease per RECIST 1.1 only.. Duration of remission (DOR) after administration. --- C18S ---

Progression Free Survival (PFS) is defined as the time from the date of first infusion of the LCAR-C18S to the first documented disease progression (according to RECIST 1.1) or death (due to any cause), whichever occurs first.. Overall Survival (OS) after administration. --- C18S ---

Overall Survival (OS) is defined as the time from the date of first infusion of LCAR-C18S to death of the subject.. Disease control rate (DCR) after administration. --- C18S ---

Time to Response (TTR) is defined as the time from the date of first infusion of LCAR-C18S to the date of the first response evaluation of the subject who has met all criteria for PR or better.. Inclusion Criteria: 1. --- C18S ---

Primary Outcomes

Description: Dose-limiting toxicity (DLT) refers to a drug-related toxicity during treatment with the drug, the severity of which is clinically unacceptable, limiting the further escalation of drug dose. An adverse event refers to any untoward medical occurrence in a clinical investigation subject administered a pharmaceutical product (investigational or non-investigational), which does not necessarily have a causal relationship with the treatment.

Measure: Dose-limiting toxicity (DLT) and incidence, severity, and type of treatment-emergent adverse events (TEAEs)

Time: 90 days post infusion

Description: Maximum tolerated dose (MTD) and recommended Phase 2 dose (RP2D)

Measure: MTD/ RP2D regimen finding

Time: 90 days post infusion

Description: Venous blood samples will be collected for measurement of CAR-T positive cellular concentration

Measure: Chimeric Antigen Receptor T (CAR-T) Positive Cell Concentration

Time: 2 years post infusion

Description: Venous blood samples will be collected to measure LCAR-C18S positive cell concentrations and the transgenic level of LCAR-C18S, at the time points when anti-LCAR-C18S antibody serum samples are evaluated

Measure: Incidence of anti-LCAR-C18S antibody and positive sample titer

Time: 2 years post infusion

Secondary Outcomes

Description: Objective Response Rate (ORR) is defined as the proportion of subjects who achieve CR or PR after treatment via LCAR-C18S cell infusion, and the objective tumor response rate will be calculated for patients with measurable disease per RECIST 1.1 only.

Measure: Overall response rate (ORR) after administration

Time: 2 years post infusion

Description: Duration of Remission (DOR) is defined as the time from the first documentation of remission (PR or better) to the first documented disease progression evidence (according to RECIST 1.1) of the responders (who achieve PR or better response).

Measure: Duration of remission (DOR) after administration

Time: 2 years post infusion

Description: Progression Free Survival (PFS) is defined as the time from the date of first infusion of the LCAR-C18S to the first documented disease progression (according to RECIST 1.1) or death (due to any cause), whichever occurs first.

Measure: Progress Free Survival (PFS) after administration

Time: 2 years post infusion

Description: Overall Survival (OS) is defined as the time from the date of first infusion of LCAR-C18S to death of the subject.

Measure: Overall Survival (OS) after administration

Time: 2 years post infusion

Description: Disease Control Rate (DCR) is defined as the proportion of patients with complete response, partial responses and stable disease.

Measure: Disease control rate (DCR) after administration

Time: 2 years post infusion

Description: Time to Response (TTR) is defined as the time from the date of first infusion of LCAR-C18S to the date of the first response evaluation of the subject who has met all criteria for PR or better.

Measure: Time to Response (TTR) after administration

Time: 2 years post infusion


HPO Nodes