CompletedPhase 2NCT00375219
Homoharringtonine (Omacetaxine Mepesuccinate) in Treating Patients With Chronic Myeloid Leukemia (CML) With the T315I BCR-ABL Gene Mutation
Studying Chronic myeloid 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
- Teva Branded Pharmaceutical Products R&D, Inc.
- Principal Investigator
- Jorge Cortes, MDUniv. of Texas M.D. Anderson Cancer Center
- Intervention
- Omacetaxine mepesuccinate(drug)
- Enrollment
- 103 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2006 – 2013
Study locations (30)
- Teva Investigational Site 003, Los Angeles, California, United States
- Teva Investigational Site 007, Jacksonville, Florida, United States
- Teva Investigational Site 006, Atlanta, Georgia, United States
- Teva Investigational Site 008, Beech Grove, Indiana, United States
- Teva Investigational Site 011, Baltimore, Maryland, United States
- Teva Investigational Site 004, Boston, Massachusetts, United States
- Teva Investigational Site 005, Buffalo, New York, United States
- Teva Investigational Site 002, The Bronx, New York, United States
- Teva Investigational Site 010, Philadelphia, Pennsylvania, United States
- Teva Investigational Site 001, Houston, Texas, United States
- Teva Investigational Site 013, Montreal, Canada
- Teva Investigational Site 009, Toronto, Canada
- Teva Investigational Site 029, Bordeaux, France
- Teva Investigational Site 021, Le Chesnay, France
- Teva Investigational Site 022, Lille, France
- +15 more locations on ClinicalTrials.gov
Collaborators
Cephalon · ChemGenex 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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