CompletedPhase 2NCT00475150
Cediranib Maleate in Treating Patients With Relapsed, Refractory, or Untreated Acute Myeloid Leukemia or High-Risk Myelodysplastic Syndrome
Studying Acute myeloid leukemia with 11q23 abnormalities
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
- National Cancer Institute (NCI)
- Principal Investigator
- Mark Juckett, MDMayo Clinic
- Intervention
- cediranib maleate(drug)
- Enrollment
- 39 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2008 – 2012
Study locations (5)
- Howard University Hospital, Washington D.C., District of Columbia, United States
- Mayo Clinic in Florida, Jacksonville, Florida, United States
- Johns Hopkins University/Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland, United States
- Wayne State University/Karmanos Cancer Institute, Detroit, Michigan, United States
- University of Wisconsin Hospital and Clinics, Madison, Wisconsin, United States
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.
Open NCT00475150 on ClinicalTrials.govOther trials for Acute myeloid leukemia with 11q23 abnormalities
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