9
Participants
Start Date
November 30, 2011
Primary Completion Date
January 31, 2012
Study Completion Date
January 31, 2012
PF-06291874 or placebo
PF-06291874 will be administered as an extemporaneously prepared suspension for all doses within the initially planned range of 3 mg to 100 mg. Correspondingly, placebo doses will be administered as suspension.
PF-06291874 or Placebo
PF-06291874 will be administered as an extemporaneously prepared suspension for all doses within the initially planned range of 300 mg to 650 mg. Correspondingly, placebo doses will be administered as suspension.
Pfizer Investigational Site, New Haven
Lead Sponsor
Pfizer
INDUSTRY