Study identifier:D3720C00015
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase I, Single-center, 2-part, Randomized, 2-way Crossover Study to Assess the Local Tolerability and Safety (Multiple-dose) and to Assess the Pharmacokinetics, Safety, and Tolerability (Single-dose) of Ceftaroline in Healthy Subjects when Ceftaroline Fosamil is Diluted in Various Infusion Volume
Healthy
Phase 1
Yes
600 mg ceftaroline fosamil in 50 ml infusion volume, Placebo in 50 ml infusion volume, 600 ceftaroline fosamil in 250 ml infusion volume, Placebo in 250 ml infusion volume, 600 mg ceftaroline in 100 ml infusion volume, Placebo in 100 ml infusion volume
All
34
Interventional
18 Years - 75 Years
Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Crossover Assignment
Masking: Double Blind
Primary Purpose: Basic Science
Verified 01 Jul 2014 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: A 600 mg ceftaroline fosamil in 50 ml infusion volume | Drug: 600 mg ceftaroline fosamil in 50 ml infusion volume IV infusion |
Placebo Comparator: B Placebo in 50 ml infusion volume | Drug: Placebo in 50 ml infusion volume IV infusion |
Experimental: C 600 ceftaroline fosamil in 250 ml infusion volume | Drug: 600 ceftaroline fosamil in 250 ml infusion volume IV infusion |
Placebo Comparator: D Placebo in 250 ml infusion volume | Drug: Placebo in 250 ml infusion volume IV infusion |
Experimental: E 600 mg ceftaroline in 100 ml infusion volume | Drug: 600 mg ceftaroline in 100 ml infusion volume IV infusion |
Placebo Comparator: F Placebo in 100 ml infusion volume | Drug: Placebo in 100 ml infusion volume IV infusion |