drugset / Trial / NCT01145560

A Study to Compare the Efficacy and Safety of 2 Dosing Regimens of IV Infusions of AZD9773 (CytoFab™) With Placebo in Adult Patients With Severe Sepsis and/or Septic Shock

NCT01145560 ↗

Phase 2 Completed 300 enrolled AstraZeneca
RandomizedParallel-groupTriple-blindTreatment

Summary

The primary purpose of this study to evaluate the effect of two different doses of AZD9773 (CytoFab™) versus placebo on ventilator free days (VFDs) over the first 28 days after the start of dosing with AZD9773 in patients with severe sepsis and/or septic shock, who are already receiving appropriate standard of care treatment for sepsis.

Timeline

Start
2010-10
Primary completion
2012-05
Completion
2012-05

Drugs

EvaluationDrugModalityDoseRoute
Subject AZD9773 Protein / enzyme biologic 50 iu/kg Intravenous
Subject AZD9773 Protein / enzyme biologic 100 iu/kg Intravenous