Phase 3 Breast Cancer Trial, Recruiting NCT07716176 Sponsor: Second Affiliated Hospital, School of Medicine, Zhejiang University Condition: Breast Cancer
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Phase 3 Breast Cancer Trial, Recruiting

NCT07716176
Recruiting Phase 3

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 26 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

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

Status
Recruiting
Phase
Phase 3
Registry
ClinicalTrials.gov
Start date
12 December 2025
Est. completion
6 December 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Proportion of patients experiencing nausea as assessed by NIC-CTC AE4.0

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov