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:
- Women between 18 and 70 years old who have not yet received any treatment for breast cancer
- People with a good general health status, able to carry out normal daily activities with little or no limitation (based on a standard health scoring system)
- People whose breast cancer has been confirmed by a lab test (biopsy) as invasive breast cancer at stage II or IIIA
- People whose cancer is hormone receptor (HR) positive and HER-2 positive
- People whose blood counts, liver function, kidney function, and heart function all fall within acceptable ranges as measured by blood tests and a heart ultrasound (confirm with trial site for specific values)
- Women who have not gone through menopause or had surgical sterilization must agree to use effective contraception during treatment and for at least 7 months after the last dose
- People who are willing to volunteer for the study and sign a consent form
Who may not be able to join:
- People whose breast cancer has spread to other parts of the body (stage IV or metastatic)
- People diagnosed with inflammatory breast cancer
- People who have previously received any anti-cancer treatment or radiation therapy for any cancer, with the exception of certain previously cured skin cancers or cervical cancer in situ
- People who are currently taking part in another clinical trial that involves anti-cancer treatments, including hormone therapy, bone-strengthening therapy, or immunotherapy
- People who had a major surgery unrelated to breast cancer within 4 weeks before joining, or who have not fully recovered from such a surgery
- People who have a history of significant lung conditions, such as lung scarring, lung inflammation, or radiation-related lung damage requiring treatment, or who are found to have such conditions during screening
- People with serious heart conditions, including a history of heart failure, uncontrolled irregular heartbeat, chest pain requiring medication, significant heart valve disease, evidence of a previous major heart attack on an ECG, or poorly controlled high blood pressure (above 180/100 mmHg)
- People who are unable to swallow or who have a bowel obstruction or other condition that would prevent them from taking or absorbing the study medication
- People with a known allergy to any of the ingredients in the study drugs, a history of immune system disorders (including HIV), other immune deficiency conditions, or a history of organ transplant
- Women who are pregnant, breastfeeding, or who have a positive pregnancy test at the start of the study, or women of childbearing age who are unwilling to use effective contraception during the trial and for 7 months after the last dose
- People with serious other health conditions that might interfere with the planned treatment, or anyone the study doctor considers unsuitable for the trial for any other 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: Zhenzhen Liu, Henan Cancer Hospital
Phone: 0371-65587005
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
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.