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Safety and Efficacy of Talactoferrin Alfa in Patients With Severe Sepsis — OASIS  

Severe Sepsis Clinical Trial

Official title:
OASIS: A Phase 2/3 Randomized, Double-blind, Placebo-controlled Study of the Safety and Efficacy of Talactoferrin Alfa in Patients With Severe Sepsis

Clinical Trial Summary

Study will evaluate the safety and potential benefit of talactoferrin (recombinant human lactoferrin) as an addition to the standard care for severe sepsis.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01273779
Study type Interventional
Source Agennix
Contact
Status Suspended
Phase Phase 2/Phase 3
Start date June 2011
Completion date December 2014
View Details
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