Phase 2 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 diagnosed with invasive breast cancer that has been confirmed by a laboratory tissue test, at specific stages involving the tumour and nearby lymph nodes but without spread to distant parts of the body
- People aged between 18 and 70 years old
- People who are generally well enough to carry out everyday activities with little or no limitation (as assessed by a standard medical scale)
- People whose breast cancer tumour has been tested for hormone receptors (ER and PR) and a protein called HER2
- People whose heart is pumping at a normal level (at least 55% efficiency, as measured by a heart scan)
- People whose cancer subtype has been confirmed through a specific type of digital analysis of tumour tissue samples
- People with triple-negative breast cancer whose tumour has been further classified using additional markers (AR, CD8, and FOXC1) (confirm with trial site)
- People who have at least one tumour that can be measured using standard imaging criteria
- People whose blood counts and organ function fall within acceptable ranges — including blood cell levels, liver function, kidney function, and other routine blood tests
- People who are not pregnant or breastfeeding, and who agree to use a medically approved form of contraception throughout the study treatment and for at least 3 months after the last dose
- People who are able to understand the study and are willing to sign a written consent form
Who may not be able to join:
- People who have previously received chemotherapy, hormone therapy, biological therapy, or radiotherapy for any reason
- People with moderate or severe heart disease, as classified by a standard medical grading system (Grade II or above)
- People with a serious active infection or other significant serious illness
- People with a known allergy or sensitivity to the study drug or any of its ingredients
- People who have had another type of cancer in the past 5 years, with the exception of certain treated cervical or skin cancers that are considered fully cured
- People who are pregnant or breastfeeding, or people of childbearing potential who are not willing to use appropriate contraception during the study
- People who have taken part in another clinical trial within 30 days before the first dose of the study drug
- People whom the trial investigators consider unsuitable for the study for any reason
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: Zhimin Shao, Professor, Fudan University
Phone: +86(021)64175590
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
Pathological complete response rate (pCR)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 7 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.