drugset / Trial / NCT00520468

Treatment of Myelodysplastic Syndrome (MDS) With Cytokine-Immunotherapy for Low-Risk MDS

NCT00520468

Phase 2 Completed 15 enrolled M.D. Anderson Cancer Center
Non-randomizedSingle-groupOpen-labelTreatment

Summary

Objectives: Primary: To evaluate the response rate of total cytokine-immunotherapy for low-risk myelodysplastic syndromes (MDS). Secondary: To evaluate response duration, survival and side effects of the treatment.

Timeline

Start
2004-06
Primary completion
2009-06
Completion
2009-06

Drugs

EvaluationDrugModalityDoseRoute
Background Cyclosporine Peptide 300 mg Oral
Background G-CSF Unknown 300 ug Subcutaneous
Background Prednisone Other / unclassified 60 mg Oral
Background epoetin alfa Protein / enzyme biologic 40000 iu Subcutaneous