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Clinical Trial Summary

The purpose of this clinical study is to evaluate the tolerability and toxicity of different dose of Anlotinib puls Gefitinib in First-line Treatment of Advanced Gene Positive Non-squamous Non-small Cell Lung Cancer , to provide a reference of dosage for Phase II clinical trials


Clinical Trial Description

This is a randomized, single -center study conducted in China to compare the tolerability and toxicity of different dose of Anlotinib Plus Gefitinib in patients of Advanced GenePositive Non-squamous Non-small Cell Lung Cancer.From low dose group up to high dose group, each one had 3 patients at least.Primary group received anlotinib 8mg. The dose of Anlotinib would increase gradually until MTD. Eligible patients were instructed to take Gefitinib 250mg orally daily for three weeks and 8mg/10mg/12mg Anlotinib orally daily on day 1 to 14 of a 21-day cycle. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03602027
Study type Interventional
Source Second Affiliated Hospital of Nanchang University
Contact Liu An wen
Phone ?13767120022?
Email awliu666@163.com
Status Not yet recruiting
Phase N/A
Start date August 1, 2018
Completion date February 1, 2019

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