Non Hodgkin Lymphoma Clinical Trial
Investigation of the Cylex® ImmuKnow® Assay
Summary
Currently, there is no accurate way of predicting the occurrence of Graft vs Host Disease (GvHD) or infection. The purpose of this study is to analyze blood with the ImmuKnow® Assay to see if doctors can detect which patients are at risk for GvHD and for getting an infection before they occur.
Eligibility Criteria
Inclusion Criteria:
Patients who are undergoing allogeneic HSCT using a myeloablative preparative regimen for any of the following disorders are eligible:
Acute leukemia
Non-Hodgkin's Lymphoma
Chronic lymphocytic leukemia
Hodgkin's disease
Multiple myeloma
Myelodysplastic Syndromes
Myeloproliferative Disorders
Aplastic Anemia
Chronic myelogenous leukemia
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There is 1 Location for this study
Indianapolis Indiana, 46202, United States
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