A 2-part Study to Assess Local Tolerability, Safety and Pharmacokinetics of Ceftaroline in Healthy Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

34

Participants

Timeline

Start Date

April 30, 2012

Primary Completion Date

September 30, 2012

Study Completion Date

September 30, 2012

Conditions
Healthy
Interventions
DRUG

600 mg ceftaroline fosamil in 50 ml infusion volume

IV infusion

DRUG

Placebo in 50 ml infusion volume

IV infusion

DRUG

600 ceftaroline fosamil in 250 ml infusion volume

IV infusion

DRUG

Placebo in 250 ml infusion volume

IV infusion

DRUG

600 mg ceftaroline in 100 ml infusion volume

IV infusion

DRUG

Placebo in 100 ml infusion volume

IV infusion

Trial Locations (1)

Unknown

Research site, London

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY

NCT01577589 - A 2-part Study to Assess Local Tolerability, Safety and Pharmacokinetics of Ceftaroline in Healthy Subjects | Biotech Hunter | Biotech Hunter