Phase 3 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 aged 18 to 85 years old
- People who have had a full surgical removal of the breast (radical mastectomy) and now need follow-up chemotherapy using a treatment combination of docetaxel and cyclophosphamide
- People with a general health and activity level rated as reasonably functional (scored 0–2 on a standard medical scale)
- People whose blood counts fall within acceptable ranges — specifically, platelets, white blood cells, and infection-fighting cells (neutrophils) all above set minimum levels
- People whose liver function tests show bilirubin and liver enzymes within acceptable limits
- People with no fluid build-up in the abdomen, no bowel blockage, normal blood clotting, and a blood protein (albumin) level of at least 30g/L
- People whose liver function is rated as "Grade A" on a standard medical scoring system
- People whose kidney function is within a normal range, either by blood test or by a calculated measure of how well the kidneys filter waste
Who may not be able to join:
- People with a local skin infection or inflammation around the ear
- People with a tendency to bleed easily or a disorder affecting blood clotting
- People with significant fluid build-up in the abdomen (severe ascites)
- People with a blockage in the bowel or digestive tract
- People experiencing a severe sudden spike in blood pressure (hypertensive crisis) or blood pressure affecting the brain
- People with serious uncontrolled conditions such as active infection or poorly controlled diabetes
- People with significant heart or blood vessel problems, including a stroke or heart attack in the past 6 months, poorly controlled high blood pressure, unstable chest pain, heart failure, or a heart rhythm problem requiring medication
- People with a history of, or signs of, central nervous system conditions such as a primary brain tumour, uncontrolled epilepsy, any past brain metastases, or stroke
- People with a known allergy or sensitivity to any of the medications used in the trial
- People who are pregnant or currently breastfeeding
- People who have other illnesses, physical impairments, or findings on examination that suggest the study treatments could be unsafe or cause serious complications
- People who are unwilling or unable to follow the requirements of the study plan
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: Juan Wang, Second Affiliated Hospital, School of Medicine, Zhejiang University
Phone: 8617816190946
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
Proportion of patients experiencing nausea as assessed by NIC-CTC AE4.0
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.