Expired Study
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Nashville, Tennessee 37203


Purpose:

This non-randomized phase II study is designed to assess the response rate and toxicity of weekly topotecan as second-line treatment in patients with relapsed or refractory metastatic colorectal cancer.


Study summary:

Upon determination of eligibility, patients will be receive: - Topotecan


Criteria:

Inclusion Criteria: To be included in this study, you must meet the following criteria: - Metastatic colorectal cancer - One previous chemotherapy for metastatic disease - Measurable or evaluable disease - Able to perform activities of daily living with assistance - Adequate bone marrow, liver, and kidney function - All patients must give written informed consent prior to study entry. Exclusion Criteria: You cannot participate in this study if any of the following apply to you: - Brain or meningeal involvement - Serious active infection or underlying medical conditions - Other active neoplasms are ineligible - Pregnant or lactating 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.


NCT ID:

NCT00193167


Primary Contact:

Principal Investigator
Anthony Greco, MD
Sarah Cannon Research Institute


Backup Contact:

N/A


Location Contact:

Nashville, Tennessee 37203
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 18, 2019

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