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.

View Eligibility Criteria

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

Study is for people with:

Non Hodgkin Lymphoma

Estimated Enrollment:

45

Study ID:

NCT00569842

Recruitment Status:

Completed

Sponsor:

Indiana University School of Medicine

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There is 1 Location for this study

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Indiana Universtiy Simon Cancer Center
Indianapolis Indiana, 46202, United States

How clear is this clinincal trial information?

Study is for people with:

Non Hodgkin Lymphoma

Estimated Enrollment:

45

Study ID:

NCT00569842

Recruitment Status:

Completed

Sponsor:


Indiana University School of Medicine

How clear is this clinincal trial information?

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