drugset / Trial / NCT02053792

A Safety and Efficacy Extension Study of a Recombinant Fusion Protein Linking Coagulation Factor IX With Albumin (rIX-FP) in Patients With Hemophilia B

NCT02053792 ↗

Phase 3 Completed 97 enrolled CSL Behring
NaSingle-groupOpen-labelTreatment

Summary

This study will examine the long-term safety and efficacy of rIX-FP for the control and prevention of bleeding episodes in children and adults with severe hemophilia B. The study will include subjects who have not previously been treated with Factor IX products, subjects who previously completed a CSL-sponsored rIX-FP lead-in study and subjects requiring major non-emergency surgery who have not previously completed a CSL-sponsored rIX-FP lead-in study. A surgical prophylaxis substudy will examine the efficacy of rIX-FP in subjects with hemophilia B who are undergoing non-emergency major or minor surgery. An additional substudy will examine the safety and PK of subcutaneous (SC) administration of rIX-FP.

Timeline

Start
2014-02-06
Primary completion
2021-06-02
Completion
2021-06-02

Drugs

EvaluationDrugModalityDoseRoute
Subject rIX-FP Protein / enzyme biologic — Intravenous

Indications