drugset / Trial / NCT01167023

Prasugrel Versus Placebo in Adult Sickle Cell Disease

NCT01167023

Phase 2 Completed 62 enrolled Eli Lilly and Company Daiichi Sankyo · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this trial is to assess the safety of Prasugrel in adult patients with sickle cell disease (SCD) by monitoring the rate and severity of hemorrhagic events requiring medical intervention compared to placebo for 30 days.

Timeline

Start
2010-07
Primary completion
2011-06
Completion
2011-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Prasugrel Small molecule 5 mg Oral

Indications