The purpose of this study is to estimate the effect of multiple oral doses of PF-03882845 on the pharmacokinetics of simvastatin and simvastatin acid in healthy, adult subjects.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
14
Single dose 20 mg simvastatin on Day 1, 30 mg PF-03882845 once daily from Days 2 to 13, the single dose 20 mg simvastatin on Day 12.
Pfizer Investigational Site
Singapore, Singapore
Composite (or Profile) of Pharmacokinetics
AUCinf, AUClast, Cmax, Tmax, t1/2 of simvastatin and simvastatin acid
Time frame: 15 days
Number of patients with adverse events as a measure of safety.
Time frame: 15 days
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