drugset / Trial / NCT01181128

Study to Evaluate the Safety, Pharmacokinetics and Efficacy of Recombinant Factor VIII Fc Fusion Protein (rFVIIIFc) in Previously Treated Subjects With Severe Hemophilia A

NCT01181128

Non-randomizedParallel-groupOpen-labelTreatment

Summary

The primary objectives of this study are: to evaluate the safety and tolerability of rFVIIIFc administered as a prophylaxis (Arm 1), weekly (Arm 2), on-demand (Arm 3), and surgical treatment regimen; to evaluate the efficacy of the rFVIIIFc tailored prophylaxis regimen (Arm 1); to evaluate the efficacy of rFVIIIFc administered as an on-demand (Arm 3) and surgical treatment regimen. The secondary objectives of this study are: to characterize the PK profile of rFVIIIFc and compare the PK of rFVIIIFc with the currently marketed product, Advate®; to characterize the range of dose and schedules required to adequately prevent bleeding in a prophylaxis regimen, maintain hemostasis in a surgical setting, or to treat bleeding episodes in an on-demand, weekly treatment, or prophylaxis setting.

Timeline

Start
2010-11
Primary completion
2012-08
Completion
2012-08

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject ADVATE Protein / enzyme biologic 50 iu/kg Intravenous
Subject Efmoroctocog Alfa Protein / enzyme biologic 10 iu/kg Intravenous
Subject Efmoroctocog Alfa Protein / enzyme biologic 25 iu/kg Intravenous
Subject Efmoroctocog Alfa Protein / enzyme biologic 50 iu/kg Intravenous
Subject Efmoroctocog Alfa Protein / enzyme biologic 65 iu/kg Intravenous

Indications