US2006014692A1PendingUtilityA1
Methods of using non-human animal Apoliprotein A-I protein
Est. expiryJul 30, 2022(expired)· nominal 20-yr term from priority
A61P 31/12A61P 9/10A61K 38/1709A61P 31/22A61K 47/6905A61P 31/18A61P 9/08A61P 31/00A61K 47/543A61P 9/00A61P 43/00A61P 31/16A61P 31/04A61P 3/06
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Claims
Abstract
The invention provides methods and compositions for treating disorders using non-human animal Apolipoprotein A-I (ApoA-I) protein. The invention provides methods and compositions for treating disorders in animals, including humans, associated with dyslipidemia, including hyperlipidemia, hyperlipoproteinemia, hypertriglyceridemia, hypercholesterolemia, HDL deficiency, ApoA-I deficiency, cardiovascular disease, atherosclerosis, restenosis, and other disorders such as septic shock and viral infections.
Claims
exact text as granted — not AI-modified1 . A method of treating a human suffering from a disorder associated with dyslipidemia, said method comprising administering to the subject an effective amount of a purified non-human animal apolipoprotein A-I protein (ApoA-I protein).
2 . The method of claim 1 wherein the disorder associated with dyslipidemia is hypercholesterolemia.
3 . The method of claim 1 wherein the disorder associated with dyslipidemia is cardiovascular disease.
4 . The method of claim 1 wherein the disorder associated with dyslipidemia is atherosclerosis.
5 . The method of claim 1 wherein the disorder associated with dyslipidemia is restenosis.
6 . The method of claim 1 wherein the disorder associated with dyslipidemia is HDL or ApoA-I deficiency.
7 . The method of claim 1 wherein the disorder associated with dyslipidemia is hypertriglyceridemia.
8 . A method of treating a subject suffering from an infection, said method comprising administering to the subject an effective amount of a purified non-human animal ApoA-I protein.
9 . The method of claim 8 wherein the infection is bacterial.
10 . The method of claim 9 wherein the infection is septic shock.
11 . The method of claim 8 wherein the infection is viral.
12 . The method of claim 11 wherein the virus is influenza.
13 . The method of claim 11 wherein the virus is human immunodeficiency virus.
14 . The method of claim 11 wherein the virus is cytomegalovirus.
15 . The method of claim 11 wherein the virus is herpes simplex virus.
16 - 21 . (canceled)
22 . The method of claim 1 or 8 wherein said subject is a human.
23 . The method of claim 1 or 8 wherein the purified non-human animal ApoA-I protein is a bovine protein.
24 . The method of claim 1 or 8 wherein the purified non-human animal ApoA-I protein is a chickens protein.
25 . The method of claim 1 or 8 wherein the purified non-human animal ApoA-I protein is a turkeys protein.
26 . The method of claim 1 or 8 wherein the purified non-human animal ApoA-I protein is a porcine protein.
27 . The method of claim 1 or 8 wherein about 0.5 mg/kg to about 100 mg/kg of the purified non-human animal ApoA-I protein is administered to said subject.
28 . The method of administering the composition of claim 27 wherein the composition is administered orally.
29 . The method of claim 27 wherein the composition is administered intravenously.
30 . The method of claim 27 wherein the composition is administered by inhalation.
31 . The method of claim 27 wherein the composition is administered once daily.
32 . The method of claim 27 wherein the composition is administered twice daily.
33 . The method of claim 27 wherein the composition is administered three times daily.
34 . The method of claim 27 wherein the composition is administered four times daily.
35 . The method of claim 27 wherein the composition is administered about once weekly.
36 . The method of claim 27 wherein the composition is administered about once monthly.
37 . The method of claim 27 wherein the composition is administered about every six months.
38 . The method of claim 27 wherein the composition is administered about once weekly for one month.Join the waitlist — get patent alerts
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