drugset / Trial / NCT01467947

Postmarketing Immunogenicity Study in HAE Subjects Treated With Berinert

NCT01467947

Phase 4 Completed 46 enrolled CSL Behring
NaSingle-groupOpen-labelTreatment

Summary

This is a prospective, international, multi-center, non-randomized, single arm, open-label, postmarketing study to investigate the formation of inhibitory anti-C1-INH antibodies in HAE subjects treated intravenously with Berinert. Individual treatment duration per subject is 9 months, irrespective of the number of treated attacks. All subjects will receive 20 IU Berinert/kg body weight per attack.

Timeline

Start
2011-11
Primary completion
2014-10
Completion
2014-10

Drugs

EvaluationDrugModalityDoseRoute
Subject CINRYZE Protein / enzyme biologic 20 iu/kg Intravenous