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| About Enrolling |
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This pleural mesothelioma study has participating centers in a number of U.S. cities. To take the next step in learning more about participating in this clinical study, please call 1-877-207-8839 and refer to study ID number 2005_010.
- Chicago, Illinois
- Las Vegas, Nevada
- Los Angeles, California
- Minneapolis, Minnesota
- New York, New York
- Norfolk, Virginia
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- Philadelphia, Pennsylvania
- Pittsburgh, Pennsylvania
- Portland, Oregon
- San Diego, California
- South Birmingham, Alabama
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This study has been registered on www.ClinicalTrials.gov under identifier NCT00128102.
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| Are You Eligible? |
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Ages eligible for study: 18 years and above
Genders eligible for study: male and female
Inclusion Criteria:
- Patient must be 18 years or older with a confirmed diagnosis of malignant pleural mesothelioma.
- Patient must have failed prior chemotherapy that included pemetrexed with either cisplatin or carboplatin.
- Patient must have adequate bone marrow and liver and kidney function.
- Patient must be capable of self-care and out of bed for more than 50% of waking hours.
- Patient must have ability to swallow pills.
Exclusion Criteria:
- Patient has been treated with another investigational agent that has similar properties.
- Patient has an active infection within 2 weeks of the start of study drug, or had treatment with intravenous antibiotic, antiviral, or antifungal medications within 2 weeks of the start of study drug.
- Patient is pregnant or breast feeding.
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