drugset / Trial / NCT02492984

PF-05208756, Moroctocog Alfa (AF-CC), Xyntha For Hemophilia A

NCT02492984

Phase 4 Completed 85 enrolled Pfizer
NaSingle-groupOpen-labelTreatment

Summary

An open-label, single-arm, post- authorization pragmatic clinical trial on the safety and efficacy of Xyntha (Moroctocog-alfa (AF-CC), Recombinant FVIII) in subjects with hemophilia A in usual care settings in China for approximately 6 months or or approximately 50 exposure days whichever occurs first

Timeline

Start
2015-04
Primary completion
2016-07
Completion
2016-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Moroctocog alfa Protein / enzyme biologic Intravenous

Indications