drugset / Trial / NCT00303472

Determination of Safe Dose of Romiplostim (AMG 531) in Patients With Myelodysplastic Syndromes (MDS)

NCT00303472

Phase 2 Completed 72 enrolled Amgen
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety and tolerability of romiplostim in thrombocytopenic patients with low or Intermediate-1 risk MDS. In addition, the study will evaluate the platelet response to romiplostim.

Timeline

Start
2006-02
Primary completion
2008-05
Completion
2008-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Romiplostim Peptide 300 ug Subcutaneous
Subject Romiplostim Peptide 700 ug Subcutaneous
Subject Romiplostim Peptide 750 ug Subcutaneous
Subject Romiplostim Peptide 1000 ug Subcutaneous
Subject Romiplostim Peptide 1500 ug Subcutaneous