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  Patient Recruitment - Pure Red Cell Aplasia
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Research Studies        
Daclizumab for Pure Red Cell Aplasia   Rituximab (Rituxan) for Pure Red Cell Aplasia   Stem Cell Transplant for Patients with Pure Red Cell Aplasia

Pure Red Cell Aplasia Research Study

Daclizumab for Pure Red Cell Aplasia

If you or someone you know has been diagnosed with Pure Red Cell Aplasia, you may be able to participate in a clinical trial evaluating a new immunosuppressive therapy. Hematologists are evaluating whether daclizumab, a genetically engineered human monoclonal antibody, can increase blood counts, reduce anemia symptoms, and/or reduce dependence on immunosuppressive medications and transfusions.

To find out if you qualify , please contact our research coordinator at (301) 594-4180 or email us at BloodStudy@nhlbi.nih.gov

 
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Pure Red Cell Aplasia Research Study

Rituximab (Rituxan) for Pure Red Cell Aplasia

If you have been diagnosed with Pure Red Cell Aplasia, you may be able to participate in a clinical trial evaluating a new immunosuppressive therapy. Hematologists are evaluating whether rituximab (Rituxan), a genetically engineered monoclonal antibody therapy, can increase blood counts, reduce anemia symptoms, and/or reduce dependence on immunosuppressive medications and transfusions. If you are determined eligible to participate, you will be treated with an infusion of rituximab once every week for a total of 4 doses and then followed to evaluate for response

To find out if you qualify, please contact our research coordinator at (301) 594-4180 or email us at BloodStudy@nhlbi.nih.gov


 
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Protocol Information

Disease and Treatment Information

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Pure Red Cell Aplasia Research Study

Stem Cell Transplant for Patients with Pure Red Cell Aplasia

If you have been diagnosed with pure red cell aplasia, you may be able to participate in a stem cell transplant clinical trial designed to evaluate methods to decrease graft-versus-host disease, promote engraftment, and improve immune system recovery following a bone marrow stem cell transplant procedure.

You must have an HLA-matched family member to participate. You will be given chemotherapy followed by a transfusion of stem cells and lymphocytes from your donor, which will replace your immune system with the immune system of your healthy donor. Post-transplant therapy is designed to reduce the risk of graft-versus-host disease.

We do the blood testing free of charge to see if your family member is a match. We pay for all medical costs related to the transplant procedure. You must be available to live near NIH for approximately 3 months. We also provide a daily allowance to help with living expenses while you are on the study and living away from home.

To inquire about eligibility, contact our research coordinator (301) 594-8013 or by e-mail: BloodStudy@nhlbi.nih.gov
 
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Protocol Information

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