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Clinical Trial Summary

The primary objective of this study is to compare progression-free survival (PFS) of patients with metastatic triple-negative breast cancer randomised to treatment with standard chemotherapy plus moxifloxacin or placebo.


Clinical Trial Description

This is a multicenter, randomised, double-blind, placebo-controlled, phase 3 trial. The main purposes of this study are to examine the efficacy and safety of standard chemotherapy plus moxifloxacin or placebo as first-line treatment in patients with metastatic triple-negative breast cancer. This study is designed to recruit up to 228 subjects. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04722978
Study type Interventional
Source Sun Yat-sen University
Contact Zhong-yu Yuan, M.D.
Phone 862087342794
Email yuanzhy@sysucc.org.cn
Status Recruiting
Phase Phase 3
Start date April 20, 2021
Completion date February 2025

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