Phase 2 Breast Cancer Trial, Recruiting NCT06107673 Sponsor: Hebei Medical University Fourth Hospital Condition: Breast Cancer
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Phase 2 Breast Cancer Trial, Recruiting

NCT06107673
Recruiting Phase 2

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 given written consent to take part in the research
  • Women who have gone through menopause and have been diagnosed with invasive breast cancer
  • People whose cancer is at a specific stage — the tumour is a certain size, cancer has spread to nearby lymph nodes, but has not spread to distant parts of the body (clinical stage T1-3N1M0 — confirm with trial site)
  • People whose cancer test results show strong hormone receptor (ER) positivity and no HER2 protein overexpression, confirmed through specific laboratory tests
  • People who have not yet received any treatment for their breast cancer
  • People with a healthy heart, with heart pumping function (LVEF) at 50% or above, and no significant heart disease
  • People who are in good general health and able to carry out normal daily activities with little or no limitation, and fit enough to receive chemotherapy
  • People whose recent blood test results (within the past week) show healthy levels of white blood cells, neutrophils, platelets, and haemoglobin
  • People whose recent liver and kidney function test results (within the past week) are within an acceptable range
  • People who test negative for pregnancy before joining the trial, and who are willing to use medically accepted contraception during the study if there is any chance of pregnancy
  • People who are likely to follow the trial schedule and requirements consistently

Who may not be able to join:

  • Women who are pregnant, breastfeeding, or who test positive for pregnancy at the start and are not willing to use effective contraception during the study
  • People with a known history of severe allergic reactions to any of the trial drugs, or any clearly documented drug allergy
  • People who have cancer in both breasts, or who have inflammatory breast cancer
  • People whose breast cancer has already spread to distant parts of the body (stage IV) at the time of diagnosis
  • People with a history of heart failure, unstable chest pain (angina), irregular heartbeat, or heart attack
  • People who currently have an active lung condition, including lung inflammation or scarring of the lungs
  • People who currently have a serious liver condition such as acute or severe hepatitis, or a liver disease affecting blood clotting; people with certain hepatitis B markers in their blood may need to meet an additional virus level requirement (confirm with trial site)
  • People with any other serious illness or ongoing health condition that could affect safety or interfere with taking part in the study, such as an active or uncontrolled infection
  • People who have or have had another type of invasive cancer that could affect how the study results are measured
  • People who have previously received chemotherapy, hormone therapy, or anti-HER2 biological therapy for breast cancer (routine diagnostic biopsy is not considered treatment for this purpose)
  • People who have had major surgery within the four weeks before joining, or who have significant unresolved health issues
  • People whose tumour cannot be measured during the course of treatment
  • People who the trial doctors consider unsuitable 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.

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 21 July 2026
Phase 2: approximately ~30% 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

Phone: 15830981676

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 2
Sponsor
Hebei Medical University Fourth Hospital
Registry
ClinicalTrials.gov
Start date
30 September 2023
Est. completion
1 December 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Percentage of Participants With Complete Radiologic Response or Partial Radiological Response: Radiological Response

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: 21 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