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[Cleveland] => https://www.survivornet.com/cleveland/
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[Dallas / Ft. Worth] => https://www.survivornet.com/dallas-ftworth/
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HuMax-CD20 in Chronic Lymphocytic Leukemia Summary The purpose of this trial is to determine the safety and efficacy of HuMax-CD20 as a treatment for Chronic Lymphocytic Leukemia.
View Eligibility Criteria Eligibility Criteria Inclusion Criteria: Chronic Lymphocytic Leukemia Circulating lymphocytes above a specific level Circulating lymphocytes showing certain markers Exclusion Criteria: Previous treatment with rituximab or alemtuzumab within 6 months prior to enrollment in study. Previous stem cell transplant ation. Received any of the following treatments within 4 weeks prior to entering this trial: A) Anti-cancer therapy, B) Glucocorticoids unless less than 10 mg per day, C) Radiotherapy. HIV positivity. Hepatitis B or hepatitis C. Other cancerous diseases, except certain skin cancers and cervix cancer. Certain serious medical conditions, including kidney or liver disease, some psychiatric illnesses, and stomach, heart, hormonal, nerve or blood diseases. Participation in another trial with a different new drug 4 weeks prior to enrollment in study. Current participation in any other clinical study. Pregnant or breast-feeding women. Women of childbearing age who are unable or unwilling to use adequate contraception.
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There is 1 Location for this study
University of Iowa, Hospitals and Clinics Iowa City Iowa, 52242, United States
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