CompletedPhase 2NCT00083187
VNP40101M in Treating Patients With Acute Myelogenous Leukemia or High-Risk Myelodysplasia
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
- Vion Pharmaceuticals
- Principal Investigator
- Francis J. Giles, MDM.D. Anderson Cancer Center
- Intervention
- hydroxyurea(drug)
- Enrollment
- 230 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2005 – 2008
Study locations (5)
- Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, Maryland, United States
- Duke Comprehensive Cancer Center, Durham, North Carolina, United States
- M.D. Anderson Cancer Center at University of Texas, Houston, Texas, United States
- Marseille Institute of Cancer - Institut J. Paoli and I. Calmettes, Marseille, France
- King's College Hospital, London, England, United Kingdom
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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