drugset / Trial / NCT01128881

IMMUNINE Pre-Treatment Study

NCT01128881 ↗

Phase 4 Completed 57 enrolled Baxalta now part of Shire
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The primary objective of this study is to prospectively document the exposure to IMMUNINE and to monitor FIX inhibitors over a period of approximately 20 to 50 exposure days while receiving prophylactic treatment in up to 50 previously treated patients (PTPs) aged 12-64 years and approximately 20 pediatric PTPs up to 11 years of age with severe (FIX level \< 1%) or moderately severe (FIX level \<= 2%) hemophilia B who are planned to enter BAX326 study 250901, provided all eligibility criteria are met. In addition, this study will evaluate the efficacy, safety, immunogenicity, thrombogenicity, and health-related quality of life (HR QoL) of these subjects.

Timeline

Start
2010-05-31
Primary completion
2012-08-28
Completion
2012-08-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Factor IX Concentrate Protein / enzyme biologic 20 iu/kg Intravenous
Subject Factor IX Concentrate Protein / enzyme biologic 40 iu/kg Intravenous

Indications