drugset / Trial / NCT00840086

Safety and Efficacy of Turoctocog Alfa in Haemophilia A Subjects

NCT00840086

Phase 3 Completed 150 enrolled Novo Nordisk A/S
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This trial is conducted in Asia, Europe, and North and South America. The trial consists of a main trial and a sub-trial. The main trial investigates safety and efficacy of turoctocog alfa (recombinant factor VIII, rFVIII (N8)) in haemophilia A subjects, while the sub-trial investigates safety and efficacy of turoctocog alfa in prevention and treatment of bleeding episodes during surgical procedures.

Timeline

Start
2009-04
Primary completion
2011-09
Completion
2011-09

Drugs

EvaluationDrugModalityDoseRoute
Subject turoctocog alfa Protein / enzyme biologic 20 iu/kg Intravenous
Subject turoctocog alfa Protein / enzyme biologic 40 iu/kg Intravenous
Subject turoctocog alfa Protein / enzyme biologic 50 iu/kg Intravenous