Clinical trial
VNP40101M in Treating Patients With Acute Myelogenous Leukemia or High-Risk…
NCT00083187 · Vion Pharmaceuticals, Industry · Completed
Key facts
| NCT number | NCT00083187 |
|---|---|
| Title | VNP40101M in Treating Patients With Acute Myelogenous Leukemia or High-Risk Myelodysplasia |
| Official title | A Phase II Study of VNP40101M For Patients With Acute Myelogenous Leukemia Or High-Risk Myelodysplasia |
| Lead sponsor | Vion Pharmaceuticals, Industry |
| Status | Completed |
| Phase | Phase 2 |
| Study type | Interventional |
| Conditions | Leukemia, Myelodysplastic Syndromes, Myelodysplastic/Myeloproliferative Neoplasms |
| Intervention type | Drug |
| Interventions | hydroxyurea, laromustine |
| Enrollment | 230 |
| Start date | Nov 1, 2005 |
| Primary completion | Jan 1, 2007 |
| Completion | Aug 1, 2008 |
| First posted | May 17, 2004 |
| Last update posted | Jul 18, 2013 |
| Countries | France, United Kingdom, United States |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: