SOLID DISPERSIONS OF RIFAXIMIN FOR THE TREATMENT OF OVERT HEPATIC ENCEPHALOPATHY
Provided herein are solid dispersions comprising rifaximin and methods of using the same for the treatment of Overt Hepatic Encephalopathy and complications associated with cirrhosis.
1 . A method of treating Overt Hepatic Encephalopathy (OHE) in a patient in need thereof comprising administering to the patient at least one rifaximin SSD IR tablet comprising about 40 mg of rifaximin.
2 . The method of claim 1 , wherein the at least one rifaximin SSD IR tablet is administered until the patient's Hepatic Encephalopathy Grading Instrument (HEGI) score or West Haven Criteria (WHC) score is reduced by at least one grade, or at least two grades, or at least three grades.
3 . The method of claim 1 , wherein the at least one rifaximin SSD IR tablet is administered until the patient's Hepatic Encephalopathy Grading Instrument (HEGI) score or West Haven Criteria (WHC) score is reduced from grade 4 to grade 3 or from grade 3 to grade 2 or from grade 2 to grade 1.
4 . A method of preventing complications of liver cirrhosis or all-cause mortality, or both, in a patient with liver decompensation comprising administering to the patient at least one rifaximin SSD IR tablet comprising about 40 mg of rifaximin.
5 . The method of claim 4 , wherein the complications of liver cirrhosis comprise one or more of hepatic encephalopathy (HE), esophageal variceal bleeding (EVB), spontaneous bacterial peritonitis (SBP), and hepatorenal syndrome (HRS).
6 . The method of claim 4 , wherein the patient has documented medically controlled non-refractory ascites.
7 . The method of claim 4 , wherein the patient has not previously experienced spontaneous bacterial peritonitis (SBP), esophageal variceal bleeding (EVB), or hepatorenal syndrome (HRS) prior to treatment.
8 . The method of claim 4 , wherein said method further comprises reducing the risk of hospitalizations associated with complications of liver cirrhosis or all-cause mortality, or both.
9 . A method of delaying the onset of overt hepatic encephalopathy (OHE) in patients with liver decompensation comprising administering to the patient at least one rifaximin SSD IR tablet comprising about 40 mg of rifaximin.
10 . The method of claim 9 , wherein liver decompensation comprises cirrhosis of the liver and medically controlled ascites.
11 . The method of claim 10 , wherein the ascites are medically controlled for a period of at least 30 days.
12 . The method of claim 10 , wherein cirrhosis of the liver is determined by one or more of histopathological evidence of cirrhosis, transient elastography, the presence of esophageal varices, and thrombocytopenia characterized by a blood platelet level of less than 150,000 in a patient with chronic liver disease.
13 . The method of claim 9 , wherein the patient has a Child-Pugh B Classification score of from 7 to 9 without OHE prior to treatment.
14 . The method of claim 9 , wherein the patient has a Model End Stage Liver Disease-Sodium (MELD-Na) score of less than 15 prior to treatment.
15 . The method of claim 9 , wherein the patient has a Conn (West Haven Criteria) score of less than 2 prior to treatment.
16 . The method of claim 9 , wherein OHE comprises a Conn score of 2 or higher.
17 . The method of claim 9 , wherein the patient does not require paracentesis.
18 . The method of claim 1 , wherein the at least one rifaximin SSD IR tablet is administered to the patient for at least one day, or at least two days, or at least 3 days, or at least 4 days, or at least 5 days, or at least 6 days, or at least 7 days, or at least 8 days, or at least 9 days, or at least 10 days, or at least 11 days, or at least 12 days, or at least 13 days, or at least 14 days.
19 . The method of claim 1 , wherein the at least one rifaximin SSD IR tablet is administered to the patient once a day, twice a day, or three times a day.
20 . The method of claim 1 , wherein the method further comprises administering lactulose to the patient.