TERLIPRESSIN COMPOSITIONS AND THEIR METHODS OF USE
Methods are disclosed of treating or preventing hypotension (e.g., neurogenic orthostatic hypotension or postprandial hypotension) or portal hypertension (e.g., bleeding esophageal varices associated with portal hypertension) or ascites (e.g., ascites associated with liver cirrhosis), by oral administration to affected subjects of compositions comprising a therapeutically effective amount of terlipressin or a pharmaceutically acceptable salt thereof.
1 .- 60 . (canceled)
61 . A method of treating a subject suffering from hypotension, the method comprising orally administering a pharmaceutical composition configured as a tablet or capsule comprising a therapeutically effective amount of terlipressin or a pharmaceutically acceptable salt thereof.
62 . The method of claim 61 , wherein the hypotension is orthostatic hypotension or postprandial hypotension.
63 . The method of claim 61 , wherein the tablet or capsule is administered 1, 2, 3 or 4 times daily.
64 . The method of claim 61 wherein the tablet or capsule is administered 1, 2 or 3 times daily.
65 . The method of claim 61 , wherein the tablet or capsule is administered 2 times daily.
66 . The method of claim 61 , wherein multiple tablets or capsules are administered 2 times daily.
67 . The method of claim 61 , wherein the tablet or capsule is administered 3 times daily.
68 . The method of claim 61 , wherein 2, 3 or 4 tablets or capsules are administered 3 times daily.
69 . The method of claim 61 , wherein the tablet or capsule comprises 5 mg to 30 mg terlipressin or a pharmaceutically acceptable salt thereof.
70 . The method of claim 61 , wherein the tablet or capsule comprises about 10 mg to about 30 mg terlipressin or a pharmaceutically acceptable salt thereof.
71 . The method of claim 61 , wherein the tablet or capsule comprises 15 mg to 25 mg terlipressin or a pharmaceutically acceptable salt thereof.
72 . The method of claim 61 , wherein the tablet or capsule comprises 18 mg to 22 mg terlipressin or a pharmaceutically acceptable salt thereof.
73 . The method of claim 61 , wherein the tablet or capsule comprises 20 mg terlipressin or a pharmaceutically acceptable salt thereof.
74 . The method of claim 61 , wherein the subject is administered 5 mg to 100 mg terlipressin or a pharmaceutically acceptable salt thereof daily.
75 . The method of claim 61 , wherein the subject is administered at least 10 mg, 20 mg, 30 mg, 40 mg, 50 mg, or at least 60 mg terlipressin or a pharmaceutically acceptable salt thereof daily.
76 . The method of claim 61 , wherein the terlipressin or a pharmaceutically acceptable salt thereof is administered for about one day to about 12 months.
77 . The method of claim 61 , wherein the terlipressin dose is increased over about one day to about 12 months.
78 . The method of claim 61 , wherein the administration provides reduced side effects relative to intravenous administration of terlipressin.
79 . The method of claim 61 , wherein the method provides greater patient compliance relative to intravenous administration of terlipressin.
80 . The method of claim 61 , wherein the hypotension is neurogenic orthostatic.
81 . The method of claim 61 , wherein the hypotension is post-prandial.
82 . The method of claim 80 , wherein oral terlipressin is administered in combination with a therapeutically effective amount of fludrocortisone.
83 . The method of claim 80 , wherein oral terlipressin is administered in combination with a therapeutically effective amount of fludrocortisone, midodrine, pyridostigmine, droxidopa, erythropoietin, ampreloxetine, or a combination thereof.
84 . The method of claim 81 wherein oral terlipressin is administered in combination with a therapeutically effective amount of guar gum, acarbose, midodrine, droxidopa, ampreloxetine, or a combination thereof.