CompletedPhase 2NCT00038610
Study of Hyper-CVAD Plus Imatinib Mesylate for Philadelphia-Positive Acute Lymphocytic Leukemia
Studying Classic hairy cell leukemia
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
- Naval Daver, MD, M.DM.D. Anderson Cancer Center
- Intervention
- Imatinib Mesylate(drug)
- Enrollment
- 54 enrolled
- Eligibility
- 15 years · All sexes
- Timeline
- 2001 – 2014
Study locations (1)
- UT MD Anderson Cancer Center, Houston, Texas, United States
Collaborators
Novartis Pharmaceuticals
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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