Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 1:01 AM
Ignite Modification Date:
2025-12-25 @ 1:01 AM
NCT ID:
NCT01088893
Eligibility Criteria:
Inclusion Criteria:
* Women aged ≥ 18 years;
* Histologically and/or cytologically confirmed invasive ductal or lobular breast cancer;
* Tumor of 3 cm or greater at time of diagnosis
* Measurable primary tumor after neoadjuvant treatment before randomization
* No prior chemotherapy for breast cancer;
* ECOG performance status ≤1 or Karnofsky performace status ≥ 70%
* Adequate liver/renal function
* Able to swallow whole tablets.
* Able to give written informed consent
* Able to follow prescription instructions reasonably well
Exclusion Criteria:
* Male patient
* Prior history of other malignancy within 5 years of study entry, aside from contralateral breast carcinoma, appropriately treated cervical carcinoma in situ, or adequately treated basal or squamous cell carcinoma of the skin
* Distant metastasis, including skin involvement beyond the breast area
* Other severe acute or chronic medical or psychiatric condition, or laboratory abnormality that would impart, in the judgment of the investigator, excess risk associated with study participation or study drug administration, or which, in the judgment of the investigator, would make the patient inappropriate for entry into this study
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT01088893
Study Brief:
Protocol Section:
NCT01088893