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Clinical Trial Summary

The reason for this study is to see if the CD73 inhibitor HLX23 alone is safe and effective in participants with advanced solid cancer.


Clinical Trial Description

An open-label, dose escalation, first-in-human, phase 1 clinical study to investigate the safety, tolerability and to determine the maximum tolerated dose and recommended phase 2 dose of HLX23 (recombinant anti-CD73 humanized monoclonal antibody) in patients with advanced or metastatic solid tumors ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04797468
Study type Interventional
Source Shanghai Henlius Biotech
Contact
Status Withdrawn
Phase Phase 1
Start date July 18, 2022
Completion date January 13, 2023

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