The primary objective of this study is to characterize the steady state plasma
The primary objective of this study is to characterize the steady state plasma PK of rifaximin (550 mg BID) in subjects with severe hepatic impairment (MELD 19 to 25 and MELD \>25), as well as healthy subjects with normal hepatic function.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
5
Rifaximin 550 MG BID
Valeant Site 01
San Antonio, Texas, United States
Maximum Observed Plasma Concentration (Cmax)
Maximum observed plasma concentration (Cmax) of rifaximin and 25-desacetyl rifaximin, if measurable
Time frame: 7 days
Time of the Maximum Concentration (Tmax)
Time of the maximum concentration (Tmax) of rifaximin and 25-desacetyl rifaximin, if measurable
Time frame: 7 days
Area Under the Plasma Concentration Versus Time Curve (AUC) During the 12-hour Dose Interval
Area under the plasma concentration versus time curve (AUC) during the 12-hour dose interval of rifaximin and 25-desacetyl rifaximin, if measurable
Time frame: 7 days
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