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Clinical Trial Summary

This is a single-arm, Phase II clinical study to explore the efficacy and safety of dalpiciclib combined with fluvestrant and compound gossypol acetate tablets in advanced HR-positive and HER2-negative breast cancer after CDK4/6 treatment failed.


Clinical Trial Description

Dalpiciclib: According to the standard dose, 150mg orally for three weeks and stop for one week. Fluvestrant: At the standard dose, 500mg once every four weeks. A further 500mg dose two weeks after the first dose. Compound gossypol acetate tablets: 20mg once a day. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06133088
Study type Interventional
Source Zhejiang Cancer Hospital
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Status Recruiting
Phase Phase 2
Start date August 1, 2023
Completion date August 31, 2025