61
Participants
Start Date
February 28, 2011
Primary Completion Date
July 31, 2011
Study Completion Date
July 31, 2011
PF-04937319
Subjects will be dosed with PF-04937319 for 14 days. The doses planned are 10, 30, 100 and 300 mg QD. All doses will be administered as tablets (10 and 100 mg strengths). In each Cohort, 9 patients will receive PF 04937319 and 3 will receive placebo. An additional cohort of 12 patients (9 active, 3 placebo) may be performed to explore a QD or BID dose. The dose for this additional cohort could be a dose already studied or a new dose that is within the exposure stopping criteria.
Placebo
Placebo to match PF-04937319 will be provided. Subjects will be dosed for 14 days. In each cohort 9 subjects will receive PF-04937319 and 3 will receive placebo.
Miami Research Associates, South Miami
MRA Clinical Research, South Miami
Elite Research Institute, Miami
Medpace Clinical Pharmacology Unit, Cincinnati
Lead Sponsor
Pfizer
INDUSTRY