CompletedPhase 2NCT01772953
Treosulfan/Fludarabine/Low Dose TBI as a Preparative Regimen for Children With AML/MDS Undergoing Allo HCT
Studying Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent
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
- Center for International Blood and Marrow Transplant Research
- Principal Investigator
- Eneida Nemecek, MDDoernbecher Children's Hospital, Oregon Health & Science University
- Intervention
- Treosulfan(drug)
- Enrollment
- 40 enrolled
- Eligibility
- 21 years · All sexes
- Timeline
- 2013 – 2015
Study locations (23)
- Children's Hospital of Alabama/UAB, Birmingham, Alabama, United States
- Phoenix Children's Hospital, Phoenix, Arizona, United States
- City of Hope, Duarte, California, United States
- Children's Hospital Los Angeles, Los Angeles, California, United States
- Children's Hospital of Colorado, Aurora, Colorado, United States
- Children's National Medical Center, Washington D.C., District of Columbia, United States
- All Children's Hospital, St. Petersburg, Florida, United States
- Riley Hospital for Children/Indiana University, Indianapolis, Indiana, United States
- University of Michigan, Ann Arbor, Michigan, United States
- University of Minnesota, Minneapolis, Minnesota, United States
- Children's Mercy Hospital, Kansas City, Missouri, United States
- Washington University, St. Louis Children's, St Louis, Missouri, United States
- University Hospitals Case Medical Center, Cleveland, Ohio, United States
- Cleveland Clinic, Cleveland, Ohio, United States
- Nationwide Children's Hospital, Columbus, Ohio, United States
- +8 more locations on ClinicalTrials.gov
Collaborators
National Marrow Donor Program · Resource for Clinical Investigation in Blood and Marrow Transplantation (RCI BMT) · Pediatric Blood and Marrow Transplant Consortium · St. Baldrick's Foundation · medac GmbH
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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