TerminatedPHASE2, PHASE3NCT00038805
Nonmyeloablative Preparative Regimen Using Mylotarg for Patients With High Risk Acute Myeloid Leukemia (AML), Acute Lymphocytic Leukemia (ALL), Chronic Myeloid Leukemia (CML) and Myelodysplastic Syndrome (MDS)
Studying Myeloid/lymphoid neoplasm associated with FGFR1 rearrangement
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
- M.D. Anderson Cancer Center
- Principal Investigator
- Marcos de Lima, MD, PA-CUT MD Anderson Cancer Center
- Intervention
- Mylotarg(drug)
- Enrollment
- 3 enrolled
- Eligibility
- 55-75 years · All sexes
- Timeline
- 2001 – 2004
Study locations (1)
- UT MD Anderson Cancer Center, Houston, Texas, United States
Collaborators
Wyeth is now a wholly owned subsidiary of Pfizer
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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