drugset / Trial / NCT02336178

Safety and Efficacy of Benefix in Patients With Hemophilia B in Usual Care Settings in China

NCT02336178 ↗

Phase 4 Completed 70 enrolled Pfizer
Open-labelTreatment

Summary

The purpose of this post-approval study is to evaluate the safety and efficacy of Benefix in subjects with hemophilia B in usual care settings in China.

Timeline

Start
2015-01
Primary completion
2016-07
Completion
2016-08

Drugs

EvaluationDrugModalityDoseRoute
Subject BeneFIX Protein / enzyme biologic — Intravenous

Indications