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 who have signed a written consent form agreeing to take part in the trial
- Women aged 18 or older
- People diagnosed with a specific type of early-stage (non-metastatic) breast cancer called triple-negative breast cancer (TNBC), meaning the cancer tests negative for certain hormone receptors and a protein called HER2, and who have already had imaging scans to check whether the cancer has spread
- People who have had surgery aimed at removing all of the cancer, where that surgery took place between 3 and 9 months before joining the trial, and who have been receiving any recommended follow-up (adjuvant) treatment for at least 12 weeks before joining
- People whose cancer is considered high-risk, meaning at least one of the following applies: the cancer did not fully disappear after chemotherapy given before surgery; the cancer was at an advanced local stage (stage IIB or III) and no pre-surgery chemotherapy was given; or the cancer has come back in the same breast area after a previous TNBC that was treated with curative intent
- People who show no signs of the cancer returning locally or spreading to other parts of the body, as assessed by their doctor
- People who have a general health status that allows them to carry out everyday activities without significant limitation (confirm with trial site what the specific health score threshold means for eligibility)
- People for whom a stored tumour tissue sample of sufficient size and quality is available
- People who are able to follow the requirements of the trial
- People who have health insurance coverage
Who may not be able to join:
- People with another serious uncontrolled illness, abnormal test results, or any other medical condition that the investigator believes would interfere with the trial
- Male participants
- People with a mental health condition or altered mental state that the investigator believes would prevent them from giving meaningful informed consent
- People who would have difficulty taking part in trial procedures for geographic, social, or psychological reasons
- People who are currently in custody or under legal guardianship
- People who have had another type of cancer in the past, unless it was a skin cancer (basal cell carcinoma), a non-invasive cancer treated with curative intent, or an early-stage cancer (stage I or II) treated with curative intent with no signs of active disease in the last five years
- People whose cancer has already spread to other parts of the body (metastatic relapse) before any molecular sign of relapse is detected through blood testing — this applies specifically to the second stage of the trial involving a particular blood test result (confirm with trial site)
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: François-Clément BIDARD, Institut Curie
Phone: 0147111515
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
Overall survival
Can't join this trial?
Data last synced from ClinicalTrials.gov: 13 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.