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Clinical Trial Summary

To explore the safety and efficacy of Eribulin plus Tucidinostat amine in patients with HR+/ HER2-advanced metastatic breast cancer


Clinical Trial Description

To explore the dose-limiting toxicity (DLT), maximum tolerated dose (MTD) and Phase II recommended dose (RP2D) of the regimen of Eribulin plus Tucidinostat , and to initially explore the safety and efficacy of Eribulin plus Tucidinostat amine in patients with HR+/ HER2-advanced metastatic breast cancer ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05335473
Study type Interventional
Source Henan Cancer Hospital
Contact Min Yan
Phone 0371-65994968
Email ym200678@126.com
Status Recruiting
Phase Phase 1/Phase 2
Start date May 13, 2022
Completion date November 1, 2025