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[Charlotte] => https://www.survivornet.com/charlotte/
[Cleveland] => https://www.survivornet.com/cleveland/
[Columbus] => https://www.survivornet.com/columbus/
[Dallas / Ft. Worth] => https://www.survivornet.com/dallas-ftworth/
[Denver] => https://www.survivornet.com/denver/
[Detroit] => https://www.survivornet.com/detroit/
[Indianapolis] => https://www.survivornet.com/indianapolis-ovarian-cancer/
[Louisville] => https://www.survivornet.com/louisville/
[Memphis] => https://www.survivornet.com/memphis/
[Minneapolis] => https://www.survivornet.com/minneapolis/
[Nashville] => https://www.survivornet.com/nashville/
[Phoenix] => https://www.survivornet.com/phoenix/
[Portland] => https://www.survivornet.com/portland/
[Salt Lake City] => https://www.survivornet.com/salt-lake-city/
[San Antonio] => https://www.survivornet.com/san-antonio/
[San Diego] => https://www.survivornet.com/san-diego/
[San Francisco] => https://www.survivornet.com/san-francisco/
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[Miami] => https://www.survivornet.com/miami-florida-multiple-myeloma-treatment/
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Study of the Safety and Efficacy of CC-5013 Treatment For Patients With Myelodysplastic Syndrome Summary To estimate the percent of patients with myelodysplastic syndrome s (MDS ) who experience erythroid response and the interval to response with daily treatment of 25 mg of CC-5013 .
View Eligibility Criteria Eligibility Criteria Diagnosis of de novo myelodysplastic syndrome of at least 12 weeks duration. Baseline mean hemoglobin < 10.0 g/dL (untransfused) and/or be transfusion dependent defined by requiring at least 4 units of RBC in the 8 weeks prior to baseline. More than 30 days must have elapsed since any previous treatment for MDS, other than transfusion. Women must not be pregnant or lactating No use of another experimental study drug within 30 dyays of baseline Understand and sign written informed consent Able to adhere to study visit schedule, understand and comply with other protocol requirements.
Check Your Eligibility
Let’s see if you might be eligible for this study.
What is your age and gender ?
There is 1 Location for this study
Arizona Cancer Center Tucson Arizona, 85724, United States
How clear is this clinincal trial information?
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