drugset / Trial / NCT00508820

An Open Label Study of Romiplostim in Adult Thrombocytopenic Subjects With ITP

NCT00508820

Phase 3 Completed 407 enrolled Amgen
NaSingle-groupOpen-labelTreatment

Summary

This protocol will provide open label romiplostim to adult thrombocytopenic subjects. Romiplostim will be administered by subcutaneous injection once per week. Dose adjustment will be based on platelet counts, and will be allowed throughout the duration of the study. Rescue therapies are allowed at any time during the study. Reductions in concurrent ITP therapies may occur at any time when platelet counts are \> 50,000.

Timeline

Start
2005-02-01
Primary completion
2011-01-01
Completion
2011-03-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Romiplostim Peptide Subcutaneous