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Clinical Trial Summary

This study aims to explore the safety, tolerability and preliminary efficacy of Anti-Mesothelin CAR-T cells in subjects with Mesothelin-positive advanced malignant solid tumors.


Clinical Trial Description

This is a single-arm, open-label, exploratory clinical study to evaluate the safety, tolerability and preliminary efficacy of Anti-Mesothelin CAR-T cells. Patients will be confirmed to have sufficient expression of mesothelin as part of a prescreening. The study comprises a dose-escalation component and a dose-expansion component. There are three cohorts in dose-expansion component. Cohort 1: To explore the effects of different conditioning chemotherapy regimens on safety, tolerability and efficacy; Cohort 2: To explore the effects of different administration modes (intravenous injection and local injection) on safety, tolerability and efficacy; Cohort 3: To explore the effects of combination immune checkpoint inhibitors on safety, tolerability and efficacy. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05783089
Study type Interventional
Source Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Contact Hong Zhao
Phone 010-87787100
Email pumc95zhao@126.com
Status Not yet recruiting
Phase Phase 1
Start date April 2023
Completion date April 2027