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Clinical Trial Summary

This project will recruit 40 EGFR-mutant metastatic non-small cell lung cancer patients who failed any EGFR tyrosine kinase inhibitors.

All recruited patients will receive 1200mg Azetolizumab administered over 60 minutes (1st cycle) and 30 minutes (2nd cycle onwards) intravenously, as well as 7.5mg/kg bevacizumab administered over 90 minutes (1st cycle), 60 minutes (2nd cycle) and 30 minutes (3rd cycle onwards) for every 3 weeks, until radiographically documented disease progression, unacceptable toxicity as judged by investigators or patient withdrawal.

The primary objective is to assess the progression-free survival of this treatment population, and to identify potential genomic and immunologic biomarkers for treatment response. Objective response rate (ORR) will be the primary efficacy endpoint.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03647956
Study type Interventional
Source The University of Hong Kong
Contact Tai-Chung Lam, FRCR
Phone +85222554352
Email lamtc03@hku.hk
Status Recruiting
Phase Phase 2
Start date October 1, 2018
Completion date April 3, 2020

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