18
Participants
Start Date
July 31, 2010
Primary Completion Date
September 30, 2010
Study Completion Date
September 30, 2010
PF-05161704 or placebo
PF-05161704 will be administered as an extemporaneously prepared suspension in the initially planned dose range of 1.5 mg to 300 mg. Correspondingly, placebo doses will be administered as suspension
PF-05161704 or placebo
PF-05161704 will be administered as an extemporaneously prepared suspension in the initially planned dose range of 1.5 mg to 300 mg. Correspondingly, placebo doses will be administered as suspension
Pfizer Investigational Site, New Haven
Lead Sponsor
Pfizer
INDUSTRY