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A Study of Prasugrel in Pediatric Participants With Sickle Cell Disease — Crescent  

Sickle Cell Disease Clinical Trial

Official title:
An Open-Label, Dose-Ranging Study of Prasugrel in Pediatric Patients With Sickle Cell Disease

Clinical Trial Summary

The purpose of this study is to determine the correct prasugrel dosage to be given to children with sickle cell disease (SCD).

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Pharmacokinetics/Dynamics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01476696
Study type Interventional
Source Eli Lilly and Company
Contact
Status Completed
Phase Phase 2
Start date November 2011
Completion date November 2012
View Details
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