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Clinical Trial Summary

The purpose of this study is to evaluate the tolerability and toxicity of different dose of anlotinib combination with concurrent chemoradiotherapy in the treatment of limited-stage SCLC patients.


Clinical Trial Description

Anlotinib is a kinase inhibitor of receptor tyrosine with multi-targets, especially for VEGFR1、VEGFR2、VEGFR3、FGFR1/2/3、PDGFRa/β c-Kit and MET. The purpose of this study is to determine the maximum tolerated dose of anlotinib when combination with concurrent chemoradiotherapy. 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04882033
Study type Interventional
Source Tianjin Medical University Cancer Institute and Hospital
Contact Xiyan Nan, Doctor
Phone +86 18811796429
Email 18811796429@163.com
Status Recruiting
Phase Phase 1
Start date May 7, 2021
Completion date July 1, 2023

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