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:
- Women with breast cancer who are between 18 and 75 years old
- People whose overall health and ability to carry out daily activities meets a standard rating of 0 or 1 on a commonly used medical scale (meaning generally active and able to care for themselves)
- People whose breast cancer has been confirmed through a tissue or cell sample to be advanced triple-negative breast cancer (a type of breast cancer that lacks three common receptors)
- People who have not yet received any systemic treatment — such as chemotherapy, targeted therapy, or immunotherapy — for their advanced triple-negative breast cancer
- People who have at least one tumour that can be measured using standard imaging criteria
- People who have decided to receive treatment with the combination of sacituzumab govitecan and toripalimab (the two drugs being studied in this trial)
Who may not be able to join:
- People who have brain metastases (cancer that has spread to the brain) causing active symptoms — such as increased pressure in the skull or seizures — that require urgent radiation therapy or surgery
- People who have previously received therapies specifically targeting HER2 or a protein called Trop-2
- People who have previously used or are currently using certain types of immune checkpoint drugs (called PD-(L)1 inhibitors), or certain types of antibody-drug combinations or medicines that affect an enzyme called topoisomerase — including drugs such as sacituzumab govitecan or Dato-DXd (confirm with trial site)
- People whom the trial investigator considers unsuitable for participating in this 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
Phone: 0086-88121122-2066
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
Progression-free Survival (PFS) as Assessed by Blinded Independent Central Review (BICR) per Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1
Can't join this trial?
Data last synced from ClinicalTrials.gov: 22 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.