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Clinical Trial Summary

To evaluate the tolerability and safety of SENL101 in patients with relapsed or refractory CD7+ hematolymphoid malignancies.


Clinical Trial Description

Main research purposes: To evaluate the tolerability and safety of SENL101 in patients with relapsed or refractory CD7+ hematolymphoid malignancies. Secondary research purposes: To preliminarily evaluate the efficacy, pharmacokinetics and pharmacodynamics of SENL101 in the treatment of patients with relapsed or refractory CD7+ hemolymphoid malignancies. Exploratory research purpose: 1. To explore the immunogenicity of SENL101; 2. T cell NK cell recovery time after treatment; 3. Other indicators of interest to researchers。 ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05398614
Study type Interventional
Source Hebei Senlang Biotechnology Inc., Ltd.
Contact Liang Huang
Phone 027-83691785
Email tongjilunli@163.com
Status Recruiting
Phase Phase 1
Start date May 1, 2022
Completion date June 30, 2024

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