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 who have been newly diagnosed with breast cancer that is both ER-negative and HER2-negative (a subtype sometimes called "triple-negative" or similar), confirmed through a tissue or cell sample test
- People with stage II or III breast cancer that doctors have assessed as suitable for chemotherapy given before surgery, with the goal of surgically removing the cancer afterward
- People whose tumor measures at least 2 cm in size based on a physical examination or imaging scan, or people with cancer that has spread to nearby lymph nodes regardless of tumor size
- People who have not yet received any treatment for this cancer
- People aged 18 years or older; both males and females are eligible
- People who are in good to fully active general health, as measured by a standard medical scoring scale (ECOG score of 0 or 1) (confirm with trial site)
- People whose blood counts, heart function, and organ function meet the required health thresholds (confirm with trial site for specific values)
- Women who could become pregnant must have a negative pregnancy test within 30 days before joining and must use effective contraception throughout the study
- People who are able to understand the study information and sign a written consent form
Who may not be able to join:
- People who have had another invasive cancer within the past 5 years, with the exception of certain treated skin cancers or a specific non-invasive cervical condition
- People who have received chemotherapy, immunotherapy, targeted therapy, or radiation treatment within the past 12 months
- People whose breast cancer has spread to other parts of the body (stage IV/metastatic)
- People who have received any vaccine within 30 days before the first study treatment
- People with serious ongoing medical conditions affecting the whole body
- People with active infections, including but not limited to HIV, hepatitis B, hepatitis C, or tuberculosis
- People with serious heart conditions, such as a heart attack, acute coronary event, or certain heart procedures within the past 6 months, or moderate-to-severe heart failure
- Women who are currently breastfeeding (breastfeeding would need to be stopped during the study)
- People with a known allergy to the study drug or any of its ingredients
- People whom the trial investigators consider unsuitable for any other medical 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: 86+18912250939
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
Pathologic complete response (pCR) rates
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.