Viewing Study NCT06180174



Ignite Creation Date: 2024-05-06 @ 7:55 PM
Last Modification Date: 2024-10-26 @ 3:16 PM
Study NCT ID: NCT06180174
Status: RECRUITING
Last Update Posted: 2023-12-28
First Post: 2023-12-12

Brief Title: Clinical Research of CD19 Targeted CAR-T Cell in RelapsedRefractory B Cell Lymphoma
Sponsor: Chongqing Precision Biotech Co Ltd
Organization: Chongqing Precision Biotech Co Ltd

Study Overview

Official Title: Phase I Clinical Study of CD19-targeting Chimeric Antigen Receptor T Lymphocyte MC-1-50 Formulation for the Treatment of RelapsedRefractory CD19-positive B-cell Non-Hodgkin Lymphoma B-NHL
Status: RECRUITING
Status Verified Date: 2023-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This is a single-arm open-label dose-escalation phase I clinical study to explore the safety tolerability and cytokinetic characteristics of MC-1-50 cell formulation and to preliminarily observe the efficacy of MC-1-50 cell formulation in subjects with relapsedrefractory CD19-positive B-cell non-Hodgkin lymphoma
Detailed Description: Based on the specific CD19-targeting CAR-T developed on the PrimeCARTM platform the cell preparation time is about 3 days which can greatly shorten the waiting time of patients improve production efficiency and reduce production costs At the same time MC-1-50 products have a high proportion of T naive cells which can play a therapeutic effect at a very small infusion dose to improve safety In this study a 33 design was adopted and four dose groups were set up with 1105kg 3105kg 5105kg and 10105kg CAR-positive cells respectively the upper limit of the total number of cells was not more than 1108 CAR-positive cells All subjects received only one infusion of MC-1-50 cells

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None