drugset / Trial / NCT00884390

Study Evaluating Safety Of Patients Switching To ReFacto AF In Usual Care Settings

NCT00884390

Phase 4 Terminated 208 enrolled Pfizer
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The study will be investigating safety in patients who switch to ReFacto AF from ReFacto and other Factor VIII products.

Timeline

Start
2009-05
Primary completion
2013-03
Completion
2013-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Moroctocog alfa Protein / enzyme biologic

Indications