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Clinical Trial Summary

This is a Phase 1, open-label, single-arm study to evaluate tolerability, safety and efficacy of RJMty19 in adult subjects with r/r B-NHL.


Clinical Trial Description

The study was based on an accelerated titration and "3+3" design with a dose-escalation phase and a dose-expansion phase, and was designed to assess the safety, maximum tolerated dose, pharmacokinetic profile, and initial efficacy of RJMty19 in subjects with r/r B-NHL after second-line treatment or above. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06314828
Study type Interventional
Source Guangdong Ruishun Biotech Co., Ltd
Contact Weili Zhao, MD,PhD
Phone +862164370045
Email zhao.weili@yahoo.com
Status Not yet recruiting
Phase Phase 1
Start date May 20, 2024
Completion date May 20, 2027

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