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Clinical Trial Summary

The purpose of the study is to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and immunogenicity of a single dose of UB-221 in healthy volunteers.


Clinical Trial Description

This is a phase I, open-label, dose-escalation study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics,and immunogenicity of a single dose of UB-221 in healthy volunteers. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04404023
Study type Interventional
Source UBP Greater China (Shanghai) Co., Ltd
Contact
Status Not yet recruiting
Phase Phase 1
Start date December 1, 2023
Completion date June 2025

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