Safety and Efficacy Study of Photopheresis With UVADEX to Prevent Graft-versus-Host Disease
Graft-versus-Host Disease
About this trial
This is an interventional prevention trial for Graft-versus-Host Disease focused on measuring Extracorporeal Photopheresis, Graft-versus-Host Disease
Eligibility Criteria
Inclusion Criteria: Patients with a diagnosis of a malignancy of the blood (e.g. leukemia) for which allogeneic bone marrow or peripheral blood stem cell transplantation is a treatment option. Patients who are candidates for a standard allogenic bone marrow transplant or PBSC transplant. Patients must have adequate renal, hepatic, pulmonary and cardiac function to enable the patient to tolerate shifts in the volumes of body fluids associated with extracorporeal photopheresis, as determined by the physician's clinical judgement. Patients must weigh at least 40 kg (88 lbs) Exclusion Criteria: Patients who have received a prior bone marrow transplant or peripheral blood stem cell transplant.
Sites / Locations
- University of Florida
- University of Chicago
- Tufts New England Medical Center
- Kansas City Cancer Center
- Cleveland Clinic Foundation
- Texas Transplant
- Royal Brisbane Hospital
- Peter MacCallum Cancer Institute
- Alfred Hospital
- Royal Melbourne Hospital
- St. Vincent's Hospital
- Hospital Azevedo Carvalho
- National Cancer Institute
- Hemocentro
- Ludwig-Maximiliano Universitaet Muenchen
- Careggi Hospital
- San Martino Hospital
- Instituto Portugues de Oncologia de Francisco Gentil
- National Cancer Institute
- Ankara University Medical School
- Hammersmith Hospital