This study will test two different formulations. The results will be used to select formulation for phase 3.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
14
Single dose of 750 mg PF-00868554 as a solution and tablets.
Pfizer Investigational Site
Brussels, Belgium
AUC inf, Cmax
Time frame: 2 days
Adverse events
Time frame: 2 days
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