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 @ 4:04 AM
Ignite Modification Date:
2025-12-25 @ 4:04 AM
NCT ID:
NCT00193102
Eligibility Criteria:
Inclusion Criteria:
To be included in this study, you must meet the following criteria:
* Metastatic breast cancer confirmed by biopsy
* Measurable or evaluable disease
* Females \> 18 years
* Able to perform activities of daily living with minimal assistance
* Life expectancy \> 3 months
* Adequate bone marrow, liver and kidney function
* All patients must give written informed consent in order to participate.
Exclusion Criteria:
You cannot participate in this study if any of the following apply to you:
* Women who are pregnant or lactating.
* Received more than 3 prior chemotherapy regimens in the metastatic setting.
* Received continuous infusion 5-fluorouracil lasting \> 120 hours.
* Received thalidomide or capecitabine as their last prior regimen.
* Preexisting moderate to severe neuropathy
Please note: There are additional inclusion/exclusion criteria. The study center will determine if you meet all of the criteria. If you do not qualify for the trial, study personnel will explain the reasons. If you do qualify, study personnel will explain the trial in detail and answer any questions you may have.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT00193102
Study Brief:
Protocol Section:
NCT00193102