drugset / Trial / NCT00123591

Safety and Preliminary Efficacy of Recombinant Activated Factor VII in Subjects With Traumatic Brain Injury

NCT00123591

Phase 2 Completed 96 enrolled Novo Nordisk A/S
RandomizedParallel-groupDouble-blindTreatment

Summary

This trial is conducted in Asia, Europe, Middle East, and North America. The primary objective of the trial is to evaluate the safety of Recombinant Activated Factor VII in patients with brain contusions. The secondary objective of the trial is to evaluate the preliminary efficacy of Recombinant Activated Factor VII in preventing early haemorrhagic progression in contusive brain injury.

Timeline

Start
2005-01
Primary completion
2006-05
Completion
2006-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Recombinant Factor VIIa Protein / enzyme biologic 40 ug/kg
Subject Recombinant Factor VIIa Protein / enzyme biologic 80 ug/kg
Subject Recombinant Factor VIIa Protein / enzyme biologic 120 ug/kg
Subject Recombinant Factor VIIa Protein / enzyme biologic 160 ug/kg
Subject Recombinant Factor VIIa Protein / enzyme biologic 200 ug/kg