Study identifier:D0620C00005
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase II, Multicentre, Randomised, Double-Blind, Placebo-Controlled, Dose Escalation Study to Assess the Safety, Tolerability and Pharmacokinetics of Intravenous Infusions of AZD9773 (CytoFab™) in Japanese Patients with Severe Sepsis and/or Septic Shock
Severe Sepsis
Phase 2
No
AZD9773, Placebo
All
20
Interventional
20 Years +
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verified 01 Sept 2014 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: 1 AZD9773 250 units/kg (1 infusion) + 50 units/kg (9 infusions) (Dose Cohort 1): AZD9773 500 units/kg (1 infusion) + 100 units/kg (9 infusions) (Dose Cohort 2) | Drug: AZD9773 A single loading dose followed by 9 maintenance doses; doses to be given every 12 hours over a period of 5 days Other Name: CytoFab™ |
Placebo Comparator: 2 | Drug: Placebo Intravenous infusion of a saline solution |