drugset / Trial / NCT00614523

Romiplostim Treatment of Thrombocytopenia in Subjects With Low or Intermediate-1 Risk Myelodysplastic Syndrome (MDS)

NCT00614523 ↗

Phase 2 Completed 250 enrolled Amgen
RandomizedParallel-groupDouble-blindSupportive care

Summary

The Data Monitoring Committee (DMC) for study 20060198 recommended that all subjects discontinue treatment of study drug and continue to be followed for long term follow-up. Amgen adopted the DMC recommendation.

Timeline

Start
2008-07-21
Primary completion
2011-03-31
Completion
2015-11-30

Outcome

Missed primary endpoint

registry Placebo vs Romiplostim; p = 0.13; Hazard Ratio (HR) 0.83 (95% CI 0.66 to 1.05) NCT00614523 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Romiplostim Peptide 250 ug Subcutaneous
Subject Romiplostim Peptide 750 ug Subcutaneous
Subject Romiplostim Peptide 1000 ug Subcutaneous