drugset / Trial / NCT00630656
Safety and Efficacy Study of Recombinant Human Lactoferrin to Treat Severe Sepsis
RandomizedParallel-groupDouble-blindTreatment
Summary
Study will evaluate the safety and potential benefit of recombinant human talactoferrin as an addition to the standard care of severe sepsis.
Timeline
- Start
- 2008-04
- Primary completion
- 2009-08
- Completion
- 2010-02
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Talactoferrin alfa | Protein / enzyme biologic | 1.5 g | Oral |