Study identifier:D3720C00010
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase I, Single Centre, Randomised, Double-blind, Placebo-controlled Parallel Group Study to Assess the Safety, Tolerability, and Pharmacokinetics of Ceftaroline after Different Intravenous Dose Regimens of Ceftaroline Fosamil to Healthy Subjects
Healthy Volunteers
Phase 1
Yes
600 mg Ceftaroline fosamil, Placebo
All
41
Interventional
18 Years - 55 Years
Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Basic Science
Verified 01 Jul 2015 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: A 600 mg Ceftaroline fosamil 1 h infusion | Drug: 600 mg Ceftaroline fosamil 1 h infusion |
Experimental: B Placebo 1 h infusion | Drug: Placebo 1 h infusion |
Experimental: C 600 mg Ceftaroline fosamil 2 h infusion | Drug: 600 mg Ceftaroline fosamil 2 h infusion |
Experimental: D Placebo 2 h infusion | Drug: Placebo 2 h infusion |