FORMULATIONS OF L-ORNITHINE PHENYLACETATE
Some embodiments of the present application are directed to oral formulations of L-ornithine phenylacetate and methods of preparing the same. These oral formulations offer alternative administration route than the standard intravenous administration of L-ornithine phenylacetate for treating hyperammonemia in patients having various acute and chronic liver diseases and disorders, for example, acute liver failure, liver cirrhosis, liver decompensation, portal hypertension, hepatic encephalopathy, or patients with urea cycle disorders.
1 .- 57 . (canceled)
58 . A product comprising an immediate release pharmaceutical formulation of about 4 g to about 6 g L-ornithine phenylacetate in a single dosage form.
59 . The product of claim 58 , wherein the immediate release pharmaceutical formulation is in the form of a liquid solution, a tablet, a capsule, a pill, pellets, or free-flowing powder.
60 . A method for treating hyperammonemia in a subject in need thereof, comprising orally administering the product of claim 58 to the subject.
61 . The method of claim 60 , wherein the product is administered twice daily.
62 . The method of claim 61 , wherein the plasma Cmax of L-ornithine is from about 18 mg/L to about 35 mg/L.
63 . The method of claim 61 , wherein the plasma Cmax of phenylacetic acid is from about 50 mg/L to about 90 mg/L.
64 . The method of claim 61 , wherein the plasma Cmax of phenylacetylglutamine is from about 30 mg/L to about 45 mg/L.
65 . The method of claim 60 , wherein the immediate release pharmaceutical formulation provides conversion of phenylacetate to phenylacetylglutamine over 24 hours of greater than about 80%.
66 . The method of claim 60 , wherein the subject has acute liver failure, chronic liver disease, liver cirrhosis or liver decompensation, hepatic encephalopathy, portal hypertension, or a urea cycle disorder.
67 . A product comprising an immediate release pharmaceutical formulation of about 4 g to about 6 g L-ornithine phenylacetate in two or more unit dosage forms.
68 . The product of claim 67 , wherein the oral pharmaceutical formulation is in two to six unit dosage forms.
69 . The product of claim 68 , wherein each unit dosage form comprises about 0.5 g to about 2.0 g L-ornithine phenylacetate.
70 . The product of claim 67 , comprising about 4 g L-ornithine phenylacetate in four unit dosage forms, each comprising about 1 g L-ornithine phenylacetate.
71 . The product of claim 67 , comprising about 6 g L-ornithine phenylacetate in six unit dosage forms, each comprising about 1 g L-ornithine phenylacetate.
72 . The product of claim 67 , wherein the immediate release pharmaceutical formulation is in the form of a liquid solution, a tablet, a capsule, a pill, pellets, or free-flowing powder.
73 . A method for treating hyperammonemia in a subject in need thereof, comprising orally administering the product of claim 67 to the subject.
74 . The method of claim 73 , wherein the product is administered twice daily.
75 . The method of claim 74 , wherein the plasma Cmax of L-ornithine is from about 18 mg/L to about 35 mg/L.
76 . The method of claim 74 , wherein the plasma Cmax of phenylacetic acid is from about 50 mg/L to about 90 mg/L.
77 . The method of claim 74 , wherein the plasma Cmax of phenylacetylglutamine is from about 30 mg/L to about 45 mg/L.
78 . The method of claim 73 , wherein the immediate release pharmaceutical formulation provides conversion of phenylacetate to phenylacetylglutamine over 24 hours of greater than about 80%.
79 . The method of claim 73 , wherein the subject has acute liver failure, chronic liver disease, liver cirrhosis or liver decompensation, hepatic encephalopathy, portal hypertension, or a urea cycle disorder.