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Clinical Trial Summary

This study is a multi-center, open-label, dose-finding phase Ib clinical study with extension phase, which is aimed at evaluating the efficacy and safety of GB226 combined with fruquintinib in treatment of relapsed or metastatic NSCLC patients with EGFR-sensitive mutations who have failed to respond to EGFR-TKI treatment,evaluating the pharmacokinetic characteristics of GB226 and fruquintinib, and the immunogenicity of GB226, and preliminarily evaluating the antitumor activity of GB226 and fruquintinib.


Clinical Trial Description

In this study, it is planned to enroll at least 42 NSCLC patients who meet relevant criteria. This study includes dose escalation phase and extension phase of the combined therapy: three combined dose groups are planned in the dose escalation phase; the dose extension phase is divided into two cohorts. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03976856
Study type Interventional
Source Genor Biopharma Co., Ltd.
Contact Shawn Yu, Master
Phone 86-010-65260820
Email shawn.yu@genorbio.com
Status Recruiting
Phase Phase 1
Start date July 23, 2019
Completion date December 2022

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