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Clinical Trial Summary

This study is designed to assess the safety and tolerability, pharmacokinetic profiles, immunogenicity of GB222 in Chinese patients with relapsed/progressive high-grade glioma; moreover, changes in cerebral edema, changes in KPS score from baseline, objective response rate (ORR), 4-month progression-free survival (PFS), overall survival (OS)will be evaluated. The dose reduction of hormone during continuous administration period will be observed.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04178057
Study type Interventional
Source Genor Biopharma Co., Ltd.
Contact Shawn Yu, Master
Phone 010-65260820
Email Shawn.Yu@genorbio.com
Status Recruiting
Phase Phase 1
Start date October 16, 2018
Completion date April 2021

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