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:
- You are between 18 and 70 years old
- You have been diagnosed with breast cancer confirmed by a tissue or cell test (biopsy or pathology)
- Your overall health and ability to carry out daily activities falls within an acceptable range for this trial (confirm with trial site)
- Your treatment plan includes radiation therapy to the chest wall or breast, with or without nearby lymph node areas
- Your treatment plan also includes at least one of the following medicines: capecitabine, a CDK4/6 inhibitor, a PARP inhibitor, an immunotherapy drug (ICI), or a HER2-targeted therapy
Who may not be able to join:
- You are male with breast cancer
- You have had an allergic reaction to any of the medicines listed above in the past
- Your treatment plan includes trastuzumab (a HER2-targeted drug) on its own, either during or after radiation therapy
- You have another serious illness or medical condition (confirm with trial site for details on what qualifies)
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: Yirui Zhai, MD, Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Phone: +86-10-87788058
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
Grade 3 adverse events
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.