49
Participants
Start Date
December 31, 2008
Primary Completion Date
March 31, 2009
Study Completion Date
March 31, 2009
Placebo
Intravenous, Placebo control for blinding, Normal Saline, Single dose
Linezolid 900 mg
Intravenous, 900 mg linezolid, single dose
Linezolid 1200 mg
Intravenous, 1200 mg linezolid, single dose
Placebo
Intravenous, Placebo control for blinding, Normal Saline, Single dose
Linezolid 600 mg
Intravenous, 600 mg linezolid, single dose
Linezolid 1200 mg
Intravenous, 1200 mg linezolid, single dose
Moxifloxacin 400 mg
Oral, 400 mg moxifloxacin, single dose
Pfizer Investigational Site, Singapore
Lead Sponsor
Pfizer
INDUSTRY