drugset / Trial / NCT00375219
Homoharringtonine (Omacetaxine Mepesuccinate) in Treating Patients With Chronic Myeloid Leukemia (CML) With the T315I BCR-ABL Gene Mutation
Phase 2
Completed
103 enrolled
Teva Branded Pharmaceutical Products R&D, Inc.
Cephalon · collabChemGenex Pharmaceuticals · collab
NaSingle-groupOpen-labelTreatment
Summary
To evaluate the safety and efficacy of subcutaneous administration of omacetaxine mepesuccinate (HHT) in achieving a clinical response in CML patients in chronic, accelerated, or blast phase who have failed prior imatinib therapy and have the T315I kinase domain gene mutation.
Timeline
- Start
- 2006-09-20
- Primary completion
- 2010-03-23
- Completion
- 2013-06-28
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Homoharringtonine | Small molecule | 1.25 mg/m2 | Subcutaneous |