drugset / Trial / NCT00630656

Safety and Efficacy Study of Recombinant Human Lactoferrin to Treat Severe Sepsis

NCT00630656 ↗

Phase 2 Completed 190 enrolled Agennix
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

EvaluationDrugModalityDoseRoute
Subject Talactoferrin alfa Protein / enzyme biologic 1.5 g Oral