drugset / Trial / NCT00116688

Open Label Extension Study of Romiplostim (AMG 531) in Thrombocytopenic Patients With Immune (Idiopathic) Thrombocytopenic Purpura (ITP)

NCT00116688

Phase 3 Completed 313 enrolled Amgen
RandomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the safety of romiplostim as a long-term treatment in thrombocytopenic subjects with ITP, to evaluate the long-term platelet response to romiplostim, and to evaluate changes in patient reported outcomes due to the use of romiplostim. Participants must have previously completed a romiplostim ITP study.

Timeline

Start
2004-08
Primary completion
2010-01
Completion
2010-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Romiplostim Peptide 1 ug/kg Subcutaneous
Subject Romiplostim Peptide 10 ug/kg Subcutaneous