drugset / Trial / NCT01128881
IMMUNINE Pre-Treatment Study
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Factor IX Concentrate | Protein / enzyme biologic | 20 iu/kg | Intravenous |
| Subject | Factor IX Concentrate | Protein / enzyme biologic | 40 iu/kg | Intravenous |