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Clinical Trial Summary

This study is an open-label, single-arm, dose escalation and dose expansion study to evaluate the safety, maximum tolerated dose, pharmacokinetic characteristics of allogeneic CD19-CAR-DNT cells (RJMty19) after infusion, and preliminary efficacy in systemic lupus erythematosus (SLE) subjects.


Clinical Trial Description

The dose escalation part (Part A) plans to enroll 9-18 subjects with refractory SLE receiving RJMty19 infusion to determine the maximum tolerated dose (MTD) and/or RP2D of RJMty19. The dose expansion part (Part B) plans to enroll 3-6 subjects. The Safety Review Committee (SRC) monitors the safety information of the subjects and evaluates the safety data of each dose group. To ensure the quality of the experiment, the sponsor and inverstigators will jointly discuss and formulate the clinical research plan before the formal experiment begins. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06340490
Study type Interventional
Source Guangdong Ruishun Biotech Co., Ltd
Contact Haicun Xie
Phone +086-18358586096
Email hcxie@wyzebiotech.com
Status Not yet recruiting
Phase Phase 1
Start date May 15, 2024
Completion date December 31, 2027

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