drugset / Trial / NCT00123591
Safety and Preliminary Efficacy of Recombinant Activated Factor VII in Subjects With Traumatic Brain Injury
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 | — |