drugset / Trial / NCT01054443

A Study to Investigate the Efficacy and Safety of Lusutrombopag (S-888711) Tablets Administered to Adults With Immune Thrombocytopenia (ITP)

NCT01054443

Phase 2 Terminated 20 enrolled Shionogi
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of this study was to assess the efficacy of 3 dose levels of lusutrombopag (0.5 mg, 0.75 mg, and 1.0 mg) and placebo on platelet count.

Timeline

Start
2010-03-18
Primary completion
2010-11-24
Completion
2010-11-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Lusutrombopag Small molecule 0.5 mg Oral
Subject Lusutrombopag Small molecule 0.75 mg Oral
Subject Lusutrombopag Small molecule 1 mg Oral