Breast Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People aged 18 or older
- People with breast cancer that has been confirmed by a laboratory test, where the cancer has not spread to distant parts of the body and has not come back in the same area
- People whose breast cancer is hormone receptor positive (HR+) and HER2 negative (HER2-) — these are specific tumour characteristics identified through testing
- People with a general health status rated between 0 and 3 on a standard medical scale (this measures how much the illness affects daily activity — confirm with trial site)
- People whose doctor is planning to treat them with a type of medication called CDK4/6 inhibitors as part of their standard follow-up treatment, in line with current medical guidelines
Who may not be able to join:
- People who are currently pregnant or breastfeeding
- People who are unable to swallow tablets, or who have a condition that affects how their body absorbs medication through the digestive system
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Wenjin Yin, M.D., Renji Hospital,School of Medicine, Shanghai Jiaotong University
Phone: 86(21)68385569
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Invasive Disease-free Survival (iDFS)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 19 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.