110
Participants
Start Date
June 30, 2010
Primary Completion Date
December 31, 2010
Study Completion Date
December 31, 2010
PF-04991532
Subjects will be dosed wtih PF-04991532 for 14 days. The tentative dosing schedule is 30, 100, 300, 1000, and 1500 mg QD, and 150 and 500 mg BID). Doses shown may be adjusted upwards or downwards and may be adjusted to include intermediate doses. All doses will be administered as tablets (10, 50, and 150 mg strengths). In each cohort 9 subjects will receive PF-04991532 and 3 will receive placebo.
Placebo
Placebo to match PF-04991532 will be provided. Subjects will be dosed for 14 days. In each cohort 9 subjects will receive PF-04991532 and 3 will receive placebo.
Pfizer Investigational Site, Miami
Pfizer Investigational Site, San Antonio
Pfizer Investigational Site, Chula Vista
Pfizer Investigational Site, Fountain Valley
Lead Sponsor
Pfizer
INDUSTRY