The effect of transporter inhibition by rifampin on the pharmacokinetics of rosuvastatin will be studied in clinical trial in White and Asian healthy volunteers.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
16
Rosuvastatin 20mg po x1
Rifampin 600mg IV infused over 30 minutes followed by rosuvastatin 20mg PO x1
CTSI Clinical Research Center, UCSF
San Francisco, California, United States
Area-under-the-concentration curve (AUC) of rosuvastatin
Time frame: Blood samples collected over a 48 hour period
Maximum plasma concentration (Cmax) of rosuvastatin
Time frame: 0, 0.5, 1, 1.5, 2, 3, 4, 6, 9, 12, 24, 32, and 48 hours post-dose
Time to concentration maximum (Tmax) of rosuvastatin
Time frame: 0, 0.5, 1, 1.5, 2, 3, 4, 6, 9, 12, 24, 32, and 48 hours post-dose
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