drugset / Trial / NCT02779569

A Clinical Trial Evaluating the Efficacy of Ultra Low Dose of Decitabine in Myelodysplastic Syndromes (MDS)

NCT02779569

RandomizedParallel-groupOpen-labelTreatment

Summary

To evaluate the safety and clinical efficacy of ultra-low-dose decitabine in Chinese MDS

Timeline

Start
2016-03
Primary completion
2019-03
Completion
2019-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Decitabine Small molecule 5 mg/m2 Subcutaneous
Subject Decitabine Small molecule 7 mg/m2 Subcutaneous
Subject Decitabine Small molecule 20 mg/m2 Subcutaneous