CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 134 enrolled
Drug / intervention
CAR-CLDN18.2 T-Cells +2 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03874897
NCT03874897Phase 1Completed

An Open Label, Single/Multiple Dose Exploratory Clinical Study to Evaluate the Safety, Efficacy, and Cytokinetics of Autologous Humanized Anti-claudin18.2 Chimeric Antigen Receptor T Cell in Advanced Solid Tumor Subjects

Peking University·interventional·Posted Mar 14, 2019·Updated Apr 30, 2024

In Brief

A Phase 1 clinical trial evaluating CAR-CLDN18.2 T-Cells, PD-1 Monoclonal Antibody, and 1 other intervention for Advanced Solid Tumor. Completed, enrolled 134 participants across 3 sites.

Detailed Summary

An open label, single/multiple dose exploratory clinical study to evaluate the safety, efficacy, and pharmacokinetics of autologous humanized anti-claudin18.2 chimeric antigen receptor T cell in advanced solid tumor.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina

Timeline

Phase 1CompletedFinished
20192020202120222023202420252026
First PostedMar 14, 2019
Enrollment StartMar 26, 2019
Primary CompletionMar 20, 2021
Study CompletionJan 26, 2024
TodayJul 1, 2026
Enrollment to primary: 2.0 yearsPosted 7.3 years ago

Interventions

CAR-CLDN18.2 T-Cellsdrug

Preconditioning with fludarabine, cyclophosphamide, based chemotherapy regimen at sub-clinical doses • Chimeric Antigen Receptor T Cells Targeting Claudin18.2

PD-1 Monoclonal Antibodydrug

Chimeric Antigen Receptor T Cells Targeting Claudin18.2 with PD-1

Chemotherapydrug

First-line systemic therapy according to physician's choice