MODULATION OF SYSTEMIC EXPOSURE TO RIFAXIMIN
The present invention relates to the effect of hepatic insufficiency on the pharmacokinetics of rifaximin. Also provided are methods of determining an appropriate dose of rifaximin for a subject suffering from hepatic insufficiency. In addition, methods of treatment are provided subjects having or susceptible to hepatic insufficiency to be treated with rifaximin.
1 . A method of treating Travelers' Diarrhea (TD) in a subject, comprising:
administering rifaximin to a subject suffering from Travelers' Diarrhea; and
informing the subject that systemic plasma exposure to rifaximin is increased in subjects suffering from hepatic insufficiency in comparison to subjects not suffering from hepatic insufficiency.
2 . The method of claim 1 , wherein the increase in systemic plasma exposure to rifaximin comprises a decrease in the terminal elimination rate constant of rifaximin.
3 . The method of claim 1 , wherein the increase in systemic plasma exposure to rifaximin comprises an increase in plasma concentration of rifaximin.
4 . The method of claim 1 , wherein the increase in systemic plasma exposure to rifaximin comprises a decrease in the clearance rate of rifaximin.
5 . The method of claim 1 , wherein administering rifaximin to the subject comprises administering 600 mg of rifaximin per day to the subject.
6 . The method of claim 5 , wherein administering 600 mg of rifaximin per day to the subject comprises administering three 200 mg tablets to the subject.
7 . The method of claim 1 , wherein informing the subject comprises providing oral instructions that systemic plasma exposure to rifaximin is increased in subjects suffering from hepatic insufficiency.
8 . The method of claim 1 , wherein informing the subject comprises providing written instructions that systemic plasma exposure to rifaximin is increased in subjects suffering from hepatic insufficiency.
9 . A method of using rifaximin for treating a patient having Traveler's Diarrhea, comprising providing a patient with rifaximin; and informing the patient or a medical care worker that systemic plasma exposure to rifaximin is increased in patients suffering from hepatic insufficiency, and that administration of rifaximin to a patient with hepatic insufficiency can affect plasma concentration, safety, or efficacy of rifaximin.
10 . The method of claim 9 , wherein the patient is provided with 200 mg tablets of rifaximin.
11 . The method of claim 9 , wherein the method comprises informing patients with model end stage liver disease that administration of rifaximin can affect plasma concentration, safety, or efficacy of rifaximin.
12 . The method of claim 9 , wherein informing the patient or the medical care worker comprises informing the patient or medical worker that rifaximin plasma concentrations (C max ) increase in patients with hepatic insufficiency.
13 . The method of claim 9 , wherein informing the patient or the medical care worker comprises informing the patient or medical worker that terminal elimination rate constant of rifaximin decreases in patients with hepatic insufficiency.
14 . The method of claim 9 , wherein patients suffering from hepatic insufficiency are patients with an elevated level of alanine aminotransferase (ALT).
15 . The method of claim 9 , wherein patients suffering from hepatic insufficiency are patients with a Child-Pugh A score.
16 . The method of claim 9 , wherein patients suffering from hepatic insufficiency are patients with a Child-Pugh B score.
17 . (canceled)
18 . (canceled)
19 . A method of treating a subject suffering from Traveler's Diarrhea, comprising administering rifaximin to the subject and advising the subject that systemic plasma exposure to rifaximin is increased in subjects suffering from hepatic insufficiency in comparison to subjects not suffering from hepatic insufficiency.
20 . (canceled)