CompletedPhase 2NCT00587054
Trial of Allogeneic Stem Cell Transplants From HLA Compatible, Related and Unrelated Donors After a Myeloablative Preparative Regimen With Hyperfractionated TBI, Thiotepa and Fludarabine For Adult Patients With Lymphohematopoietic Disorders
Studying Paroxysmal nocturnal hemoglobinuria
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Memorial Sloan Kettering Cancer Center
- Principal Investigator
- Ann Jakubowski, MDMemorial Sloan Kettering Cancer Center
- Intervention
- cytoreductive regimen followed by a CD34+E- selected allogeneic stem cell transplant(drug)
- Enrollment
- 129 enrolled
- Eligibility
- 18-55 years · All sexes
- Timeline
- 2001 – 2011
Study locations (1)
- Memorial Sloan-Kettering Cancer Center, New York, New York, United States
Collaborators
National Cancer Institute (NCI)
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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