drugset / Trial / NCT01848925

Study of SANGUINATE™ Versus Hydroxyurea in Sickle Cell Disease (SCD) Patients

NCT01848925

Phase 1 Completed 24 enrolled Prolong Pharmaceuticals
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to compare the safety of SANGUINATE™ versus Hydroxyurea in patients suffering from Sickle Cell Disease.

Timeline

Start
2013-05
Primary completion
2014-07
Completion
2014-08

Drugs

EvaluationDrugModalityDoseRoute
Comparator Hydroxyurea Other / unclassified 15 mg/kg
Subject pegylated carboxyhemoglobin bovine Protein / enzyme biologic 40 mg/ml Intravenous

Indications